|Year : 2019 | Volume
| Issue : 1 | Page : 180
Evaluation of the protective effect of cystone against cisplatin-induced nephrotoxicity in patients with cancer: A pilot study
Mohammad Reza Tamadon1, Samaneh Tirom1, Farahnaz Ghahremanfard1, Azar Baradaran2, Raheb Ghorbani3
1 Department of Internal Medicine, Semnan University of Medical Sciences, Semnan, Iran
2 Department of Pathology, Isfahan University of Medical Sciences, Isfahan, Iran
3 Social Determinants of Health Research Center, Semnan University of Medical Sciences, Semnan, Iran
|Date of Submission||15-Feb-2018|
|Date of Acceptance||16-Jul-2018|
|Date of Web Publication||09-Oct-2019|
Department of Internal Medicine, Semnan University of Medical Sciences, Semnan
Source of Support: None, Conflict of Interest: None
Introduction: Cisplatin is a widely used anti-cancer drug that is commonly administered for the treatment of various cancers. However, nephrotoxicity is the most important side effect of this drug which limits its use. This study aimed to investigate the protective effect of Cystone against nephrotoxicity induced by Cisplatin in patients with cancer. Methods: This pilot clinical trial study was conducted on 43 cancer patients treated with Cisplatin (75 mg/m2 for a period of six months). The subjects were divided into treatment group (receiving Cystone, two per 8 hours; n = 21) and control group (n = 22). The two groups were compared with each other in terms of demographic and laboratory variables. Results: In the intervention group receiving Cystone, serum creatinine-based GFR level (P = 0.453) and 24-hour urine creatinine-based GFR level (P = 0.397) did not change significantly during the studied period, but in the control group, serum creatinine-based GFR level (P = 0.013) and 24-hour urine creatinine-based GFR level (P = 0.016) significantly changed. Serum creatinine-based GFR level increased by 2.3 units in the intervention group and 10.5 units in the control group (P = 0.005) in the six months of the study. At the end of the sixth month, 24-hour urine creatinine-based GFR level increased by 2.2 units in the intervention group and 0.8 unit in the control group (P = 0.008). Conclusions: The use of Cystone resulted in more stable kidney function indices in the intervention group, as compared with the control group. Therefore, Cystone seems to have a protective effect against nephrotoxicity induced by Cisplatin in cancer patients.
Keywords: Cisplatin, cystone, neoplasm, nephrotoxicity
|How to cite this article:|
Tamadon MR, Tirom S, Ghahremanfard F, Baradaran A, Ghorbani R. Evaluation of the protective effect of cystone against cisplatin-induced nephrotoxicity in patients with cancer: A pilot study. Int J Prev Med 2019;10:180
|How to cite this URL:|
Tamadon MR, Tirom S, Ghahremanfard F, Baradaran A, Ghorbani R. Evaluation of the protective effect of cystone against cisplatin-induced nephrotoxicity in patients with cancer: A pilot study. Int J Prev Med [serial online] 2019 [cited 2019 Oct 15];10:180. Available from: http://www.ijpvmjournal.net/text.asp?2019/10/1/180/268758
| Introduction|| |
Acute renal failure is common in seriously ill hospitalized patients and its mortality rate has not changed significantly over the recent decades. Available reports indicate that acute renal failure has increased over the past two decades, and the rate of mortality in dialysis patients has exceeded 50%.
The progresses which have been made in understanding the nature of the disease have led to the production and testing of several medications and interventions, and the rate of mortality has slightly improved. Therefore, it has become important to take preventive measures to prevent the incidence and progress of acute renal failure. In recent years, many efforts have been made to produce drugs from traditional and herbal materials. Acute renal failure is mainly characterized by acute tubular necrosis.,,,,,,,,, On the other hand, a number of drugs can have adverse effects on kidney, resulting in acute renal failure and other abnormalities in patients. Some drugs, such as aminoglycosides, non-steroidal anti-inflammatory drugs, and chemotherapy drugs are commonly used to deal with this problem.,,,,,
Cisplatin (cis-diammine-di-chloro-platinum) is an anticancer drug that is widely used to treat various types of cancer. In 1969, the results of an animal experiment showed that this drug had anti-tumor properties. In addition to eliminating carcinogenic cells, this widely used medication also has deleterious effects on healthy tissues. As one of the main mechanisms of action, Cisplatin induces cell death. Cisplatin reabsorption occurs due to an increase in radical oxygen species, which results in activation of internal and external apoptotic pathways, degradation of chromosomes, and peroxidation of lipids. Nephrotoxicity is the most important side effect of Cisplatin which limits it use for the treatment of diseases. Cisplatin-induced nephrotoxicity emerges in kidney tubules, especially proximal tubules. Several mechanisms are involved in the nephrotoxicity caused by this drug, among which the most important are the production of active oxygen species and tissue oxidative damage. Active oxygen species, especially radical hydroxyl, leads to the peroxidation of fats, degradation of cell membrane, oxidation of protein and nucleic acids, and degradation of tissue, resulting in a reduction in glomerular filtration and causing acute nephrotoxicity.,,,,,,,, Cisplatin-induced nephropathy is the most important reason for reducing the dose of this drug. Some of the patients with acute renal failure are hospitalized due to the unavoidable administration of this drug. Despite the use of hydration as a factor reducing the nephrotoxicity induced by this drug, about one third of patients receiving Cisplatin would suffer from a non-reversible kidney damage.,,,, Therefore, there is an increasing global interest in reducing the nephrotoxicity induced by Cisplatin in cancer patients, as they are highly vulnerable patients.
The use of herbal medicines has a long history and it can be said that the basis of modern medicine. Many conventional drugs originate from plant sources. In many literatures has been mentioned that effectiveness of herbal medicines is resulted from antioxidants. Antioxidants are effective in prevention and treatment of many diseases, as well as the side effects of some medications.,,,,,,,,,,
Cystone, as an herbal drug, is one of the medications that have recently been tested on the patients and, as reported, it has had satisfactory results. Cystone is a well-known herbal medicine used for many years for the treatment of kidney stones and urinary tract infections. This herbal mix contains nine different types of plant extracts. Cystone has shown anti-carcinogenic effects against sarcoma in mice. The results of a study has shown that Cystone protects kidney against the toxicity induced by Cisplatin and it acts through inhibiting fat peroxidation. Therefore, several studies have investigated the effect of Cystone on the prevention of the toxic effects of Cisplatin and other factors that cause nephrotoxicity; however, not only the results have been controversial, but also many of these studies are conducted on animals.,,,,, Overall, in spite of extensive studies on the factors affecting the nephrotoxicity induced by Cisplatin which have been conducted over the past few decades, there is still insufficient knowledge about the cause and pathogenesis of this complex disorder; thus, there is not adequate knowledge basis for designing and targeting interventions for the effective prevention and treatment of this disorder. Therefore, it is of great importance to identify and assess its current status and conduct further studies to control this disorder, in order to prevent clinical symptoms or prevent the transfer from mild to severe cases. As a consequence, as the pathogenesis of Cisplatin-induced nephrotoxicity in cancer has not been clearly defined yet, and since a limited number of studies have investigated the effects of Cystone on nephrotoxicity induced by Cisplatin, it seems necessary to carry out further studies in order to clarify the relationship between the nephrotoxicity induced by Cisplatin drug and investigate the positive effects of Cystone. Hence, based on what has been mentioned so far, the study of the effects of Cystone on Cisplatin-induced nephrotoxicity in cancer patients have been assessed in a small number of studies, mainly on animal samples; even, the small number of studies, which have been conducted so far, have presented contradictory results. In addition, the impact of race, ethnicity, and geographical area on the results of studies is undeniable. Therefore, it is of great importance to conduct more clinical trials in different communities using different methods.,,,,,, The present study aimed to investigate the effect of Cystone on nephrotoxicity induced by Cisplatin in cancer patients.
| Methods|| |
This study was a clinical trial which was conducted as a pilot study because the majority of previous studies have often been performed as animal experiments and very few human studies are found in this field.
The study sample included all patients with cancer who referred to Kosar Hospital in Semnan from spring 2015 to summer 2016 to start their treatment using Cisplatin. After confirming the preliminary proposal of the project in the research council of Kosar Educational, Research, and Therapeutic Center, in Semnan, it received an ethics approval code from the Ethics Committee of the university. After explaining the details about the method and importance of this study and giving a full description of the process of study, a written consent from was given to the patients or their relatives to consent participating in the study.
Exclusion criteria were the followings:
- Previous history of kidney disease
- Concurrent use of drugs or materials inducing nephrotoxicity
- Previous history of treatment with Cisplatin
- Incidence of Cisplatin-induced complications that require discontinuation of the drug.
Primary data were collected using a checklist containing questions about demographic features, type of cancer, clinical examination, para-clinical data (white blood cell count (WBC), hemoglobin, platelet, BUN, creatinine, creatinine-based GFR, 24-hoururine-based GFR, AST, ALT, alkaline phosphatase, INR, albumin, direct bilirubin (DBil), and total bilirubin (TBil)). Then, the subjects were randomly divided into two intervention and control groups using six-member blocks, in which the members were matched in terms of age and sex.
- Intervention group: Treated with Cisplatin 75 mg/m2 in six rounds each lasting 21 days plus Cystone tablet (manufactured by the Himalayan Pharmaceutical Company, India) administered as two pills every 8 hours for 21 days
- Control group: Treated with Cisplatin 75 mg/m2 in six rounds each lasting 21 days.
Then, we compared and analyzed the measured levels of white blood cells (WBC), hemoglobin, platelets, BUN, and creatinine at the end of each round and the measured levels of creatinine-based GFR, 24-hour urine-based GFR, AST, ALT, alkaline phosphatase, INR, albumin, total bilirubin, and direct bilirubin, just at the end of the first, third, and sixth rounds of chemotherapy with Cisplatin.
Using Kolmogorov-Smirnov test, T-Student test (or Mann-Whitney test), analysis of variance with repeated measurements, and Friedman test, the collected data were analyzed at a significance level of 5%, using SPSS software version 18.
In this study, the following ethical issues were observed. The checklists were anonymous and only included figures and raw data. In addition, the subject were ensured about the confidentiality of the data. On the other hand, a written informed consent was obtained from all the subjects and they were allowed to withdraw and quit the study, at any stage, if they wished to do not participate anymore.
| Results|| |
Of the 44 patients (aged 18 to 75 years), two patients were excluded from the study due to overexpression of creatinine and one patient due to skin rash and the probable allergy to Cystone. The other patients were divided into two groups of Cystone and control groups. There was no significant difference between the two groups in terms of age, sex, and body mass index (respectively, P = 0.443, P = 0.193, P = 0.118). Gastric cancer was the most common malignancy observed in patients.
Mean and standard deviation of the level of creatinine-based GFR after the intervention, as compared with the time before the intervention, was increased by an average of 2.3 ml/min/m2in the intervention group receiving Cystone; however, it decreased by an average of 10.5 ml/min/m2in the control group. Thus, the difference was significant (P = 0.005) [Table 1].
|Table 1: Mean and standard deviation of glomerular filtration rate, creatinine and blood urea nitrogen levels in different stages of study in two groups|
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In the group treated with Cystone, the level of creatinine-based GFR did not change significantly in the six stages (P = 0.453); however, in the control group, the level of creatinine-based GFR level was significantly changed in the six stages (P = 0.013).
The mean and standard deviation of the level of 24-hour urine creatinine-based GFR at the end of the sixth month, as compared with the first month, was increased by an average of 2.2 ml/min/m2in the group treated with Cystone, while it decreased by an average of 8.0 ml/min/m2in the control group, and the difference was significant (P = 0.008) [Table 2].
|Table 2: Mean and standard deviation of glomerular filtration rate level based on 24-hour urine creatinine in different stages of study in two groups|
Click here to view
In the group treated with Cystone, the level of 24-hour urine creatinine-based GFR did not change significantly in the three stages (P = 0.397), but in the control group, the changes were significant (P = 0.016).
The changes in BUN level and the difference between the two groups were not significant in the studied stages, as compared with the time before the intervention [Table 1]. In the intervention group treated with Cystone, BUN level did not change significantly in the six stages (P = 0.186); however, in the control group, BUN levels significantly changed in the six stages (P = 0.006).
The comparison of mean and standard deviation of hemoglobin level at the end of the sixth month, as compared with the first month, showed that the mean hemoglobin level in the group treated Cystone and in the non-Cystone group (control group) decreased by an average of 0.22 g/dL and1.70 g/dl, respectively. Thus, the difference was significant (P = 0.10).
The changes in hemoglobin level were significant in the six stages both in the Cystone group (P = 0.009) and in the control group (P ≤ 0.001).
The comparison of mean and standard deviation of creatinine level at the end of the second month, as compared with the time before the intervention, showed that the creatinine level in the intervention group treated with Cystone decreased by an average of 0.05 mg/dL, while in the group that did not receive Cystone (control group) it was increased by an average of 0.05 mg/dL, and the difference was significant (P = 0.42) [Table 1]. The changes in creatinine level in 6 stages in the Cystone group were not significant (P = 0.408), but in the control group, the changes in creatinine level were significant in the six stages (P = 0.004).
The mean and standard deviation of WBC levels in the second to sixth stages of the study, as compared with the time before the intervention (stage one), did not change significantly. Changes in WBC levels were not significant in the Cystone intervention group in the six stages (P = 0.127), but the changes in WBC levels in the control group in the six stages were significant (P = 0.046).
There was no significant change in mean and standard deviation of platelet level from the second to the sixth stage of the study, as compared with the time before the intervention (stage one). Platelet level changes were significantly different in the Cystone group (P < 0.001) and the control group (P = 0.026) in all the six stages.
The changes in AST level in the two groups were not significant in the studied months, as compared with the end of the first month. There was no significant difference between the levels of AST in the group treated Cystone (P = 0.223) and the group that did not receive Cystone (P = 0.399) in the three stages.
The changes in ALT level in the two groups were not significant in the studied months, as compared with the end of the first month. There was no significant difference in ALT levels in the group treated with Cystone (P = 0.520); however, in the group that did not receive Cystone, there was a significant difference in the three stages (P = 0.399).
The changes in ALKP level in the two groups were not significant in the studied months, as compared with the end of the first month. In the group treated with Cystone (P = 0.990) and in the group that did not receive Cystone (P = 0.119), ALKP level was significantly different in the three stages.
The changes in INR level in the two groups were not significant in the studied months, as compared with the end of the first month. In the intervention group treated with Cystone (P = 0.128) and in the group that did not receive Cystone (P = 0.066), the level of INR was significantly different in the three stages.
The changes in albumin level in the two groups were not significant in the studied months, as compared with the end of the first month. In the group treated with Cystone, the level of albumin was not significantly different in the three stages (P = 0.831); however, in the group that did not receive Cystone, the level of albumin was significantly different in the three stages (P = 0.007).
The changes in total bilirubin level in the two groups were not significant in the studied months, as compared with the end of the first month. In the Cystone group (P = 0.805) and in the group that did not receive Cystone (P = 0.77), total bilirubin levels were not significantly different in the three stages.
At the end of the sixth month, as compared with the end of the first month, direct bilirubin level in the Cystone group decreased by an average of 0.6 mg/dL and while in the control group it increased by an average of 0.60 mg/dL, and the difference was significant (P = 0.049). There was no significant difference in the level of direct bilirubin between the intervention group treated with Cystone (P = 0.607) and the group that did not receive Cystone (P = 0.078).
| Discussion|| |
The present study was one of the first studies examining and evaluating the protective effect of Cystone against nephrotoxicity induced by Cisplatin in human subjects. Based on the results of a search, of all previous studies in this field, only two studies were conducted on human subjects and the other studies were carried out on animals. On the other hand, based on the results of a study conducted by El-Ghiaty et al. in 2014, it was stated that Cystone had a protective effect against Cisplatin; they also reported that the kidney function was significantly better in patients receiving Cystone than in those who did not receive this medication.
Based on the results of this study, no significant difference in the results of renal pelvic tests was not observed in the intervention group treated with Cystone during the different stages of the study. Other studies have shown that kidney failure is observed several days after Cisplatin administration with a decrease in glomerular filtration rate, an increase in blood urea nitrogen, and an increase in serum creatinine. The results of other studies have also shown that the use of Cisplatin alone for chemotherapy, without the use of protective drugs, resulted in abnormal renal test results, especially in creatinine and BUN level. The results of our study showed no significant change in the level of creatinine-based GFR in the group treated with Cystone in the six stages of the study. However, the level of creatinine-based GFR had significant changes in the control group in the six stages of the study. The results showed that at the end of the sixth month, as compared with the first month, the mean hemoglobin level was reduced by an average of 0.22 g/dl in the group treated Cystone and by an average of 1.70 g/dl in the non-Cystone group (control group) and the difference was significant. These findings are in line with the results of a study by El-Ghiaty et al., 2014. Other studies have suggested that the administration of Cisplatin without protective drugs causes direct tubular damage, which in turn results in a reduction in glomerular filtration and, ultimately leads to acute nephrotoxicity. Several studies have shown that some symptoms such as proteinuria, glycosuria, and increased plasma urea and creatinine level are observed after the incidence of acute nephrotoxicity, and the results of this study also confirmed such a finding. El-ghiaty et al. investigated kidney function in 49 patients with cancer who were under treatment through taking six rounds of Cisplatin; in that study, kidney function was measured through calculating serum creatinine, creatinine clearance, and blood urea. At the end of the study it was observed that kidney function in patients receiving Cystone was far better than that in patients who did not receive this drug, which is consistent with the results of this study. Other studies are often performed on animal subjects. In a study conducted in 2004, researchers had injected Cisplatin and Cystone into the peritoneum of male rats; at the end of the study, the results showed that the changes in kidney function in mice receiving Cystone was much lower than that in the control group. The results of a study in 2011 showed that the administration of Cystone reduced kidney dysfunction in rats treated with Cisplatin and resulted in a better level of serum creatinine at the end of treatment. However, there are other studies that used other criteria for assessing renal function and had similar results. Raom et al. showed that cats receiving Cisplatin together with Cystone had better urine output. At the end, the researchers concluded that patients receiving Cystone had better urine output and, consequently, had better kidney function after receiving Cisplatin. The induction of cell death, the activation of internal and external apoptotic pathways, chromosomal degradation and lipid peroxidation are among the main mechanisms of actions of Cisplatin. This drug, which is a commonly used drug in the chemotherapy of cancer patients, plays a special role in the development of toxicity in kidney tubules, and in particular in proximal tubule., Several other mechanisms are involved in the nephrotoxicity induced by this drug, among which the most important are the production of active oxygen species and tissue oxidative damage. Active oxygen species, especially radical hydroxyl, lead to fat peroxidation, cell membrane degradation, protein and nucleic acid oxidation, and tissue degradation, resulting in decreased glomerular filtration and acute nephrotoxicity. A number of studies have also suggested that nephropathy induced by this drug may be due to the direct effect of the drug on different stages of tubular or mitochondrial transmission, alteration in cellular structure, or the release of free radicals. Moreover, Cystone not only has anticancer effects in mice, but also protects the kidney against the toxicity induced by Cisplatin through its ability to inhibit lipid peroxidation. A number of studies has investigated the role of Cystone's components on the nephrotoxicity of the drug; for example, in a study in 2008, the effect of Rubiacardifolia, a component of Cystone, on the nephrotoxicity induced by Cisplatin was investigated. The results of the mentioned study showed that the glomerular filtration rate in mice that received this compound was significantly lower than that in the group that did not receive that component; this finings is in line with the results of our study. Nonetheless, free oxygen radicals play an important role in causing acute renal failure induced by Cisplatin. Therefore, it is not surprising to observe that Cystone, as an herbal medicine and effective antioxidant, like many other antioxidants such as vitamins C and E can reduce the nephrotoxicity induced by Cisplatin. Other studies have also indicated that other antioxidants, such as N-acetyl cysteine (NAC), can reduce the severity of Cisplatin-induced renal damage in both animals and humans. It highlights the importance of the antioxidant effect of drugs (especially Cystone which is a drug with low complications) against toxicity induced by Cisplatin. The renal damage induced by Cisplatin is caused by reactive oxygen species, and in particular hydroxyl, which lead to lipid peroxidation and protein degradation, causing tubular damage and acute nephrotoxicity; thus, one of the most important prevention factors is the amount of intracellular glutathione storage which is reduced as the result of the formation of oxidative stress induced by Cisplatin, as it reduces cellular glutathione level, and increases the activity of reactive oxygen species, and ultimately, results in tubular degeneration and acute nephrotoxicity. However, Cystone has some indirect effects which emerge through various components and paths and improve the outcomes.
In this study, there was no significant difference between the two groups treated with Cystone and the control group in terms of the underlying variables such as age, gender, and body mass index. It indicates that the subjects are homogeneous and, as a result, the effect of confounding variables (including age, gender, and body mass index) on the findings of this study are controlled. It improves the judgment and comparison between the two groups. This finding is similar to the results of a number of other valid studies;, as a number of studies have emphasized the effectiveness of age and sex on the increase in nephrotoxicity. Therefore, the homogeneity of the two studied groups in terms of these variables can be considered as one of the strengths of this study which was achieved through the selection of the subjects and implementation of the research plan.
Along with the strengths of this study, our study, like any other study, had a number of limitations. One of the most important limitations of this study was the low sample size. In addition, we analyzed the protective effects of Cystone against Cisplatin-induced nephrotoxicity only within a six-month period of treatment, which was due to lack of cooperation in patients and the limited financial resources for carrying out periodic tests. Thus, it was not possible to conduct longer-term studies, and, consequently, assess the benefits or complications of long-term use of Cystone intervention.
In order to achieve better results and operationalize the findings of the study, it might be helpful to investigate the effects of higher doses of Cystone, and assess the effects of prolonged treatment using this drug, and even the prophylactic effects of the administration of the drug long before the start of chemotherapy. Other clinical trials can help generalize the results of this study by examining the protective effects of Cystone against nephrotoxicity induced by other nephrotoxic drugs. They might also assess other groups of patients, and even those who met the exclusion criteria in our study. As our study was not a blinded trial and the control group did not receive any specific placebo, it is recommended to conduct further blinded trials using placebo for the control group to achieve better results.
| Conclusions|| |
Overall, the results of this study showed that the use of Cystone resulted in more stable kidney function indices in the intervention group, as compared with the control group. Therefore, Cystone seems to have a protective effect against nephrotoxicity induced by Cisplatin in cancer patients. It is recommended to conduct further studies to clarify the mechanism of the effect of Cystone on kidney, and also to investigate its protective effect against other nephrotoxic drugs.
Limitations of our study
Given the contradicting results of this and other studies, future studies are recommended to be conducted on the long-term effects of contrast agents on renal function.
This article is part of M.D thesis of Samaneh Tirom (# 23-6), approved by the Research Deputy of Semnan University of Medical Sciences, ethical committee (IR.SEMUMS. REC.1394.150) and registered in Iranian Registry of Clinical Trials (IRCT2016052726425N2). The authors wish to thank all staffs of the medical ward of Kowsar hospital for their cooperation in this study.
Financial support and sponsorship
This study supported and funded by the Research Deputy of Semnan University of Medical Sciences (Grant # 936).
Conflicts of interest
There are no conflicts of interest.
| References|| |
Mohamed R, Viswanatha GL. Cystone, a well-known formulation improves renal function in rats with acute renal failure induced by glycerol intoxication. Iran J Pharmacol Ther 2012;11:40-4.
Hasanvand A, Mir S, Mohammadrezaei Khorramabadi R, Darabi S. Ameliorative effect of ferulic acid on gentamicin-induced nephrotoxicity in a rat model; role of antioxidant effects. J Renal Inj Prev 2018;7:73-7.
Tamadon MR, Ardalan MR, Nasri H. World Kidney Day 2013; acute renal injury; a global health warning. J Parathyr Dis 2013;1:27-8.
Mohammadi A, Ahmadizadeh M. Effects of antioxidants on xenobiotics-induced nephrotoxicity. J Renal Inj Prev 2018;7:56-7.
Tan RZ, Liu J, Zhang YY, Wang HL, Li JC, Liu YH, et al
. Curcumin relieved cisplatin-induced kidney inflammation through inhibiting Mincle-maintained M1 macrophage phenotype. Phytomedicine 2019;52:284-94.
Nazar CM, Bashir F, Izhar S, Anderson J. Overview of management of acute renal failure and its evaluation; a case analysis. J Nephropharmacol 2015;4:17-22.
Dehghan Shahreza F. From oxidative stress to endothelial cell dysfunction. J Prev Epidemiol 2016;1:e04.
Nasri H, Amiri M. World kidney day 2017 with the theme of kidney disease and obesity. Ann Res Dial 2017;2:e01.
Akbari R, Bahadoram M, Ghorbani A, Zarghami A. Campaigning for kidney health; an experience from kidney day in Iran. Ann Res Dial 2016;1:e02.
Ibrahim ME, Chang C, Hu Y, Hogan SL, Mercke N, Gomez M, et al
. Pharmacokinetic determinants of cisplatin-induced subclinical kidney injury in oncology patients. Eur J Clin Pharmacol 2019;75:51-7.
Rao M, Rao MN. Protective effects of cystone, a polyherbal ayurvedic preparation, on cisplatin-induced renal toxicity in rats. J Ethnopharmacol 1998;62:1-6.
Amiri M. Aggravation of chronic kidney disease by inflammatory factors; a narrative review on current concepts. J Ren Endocrinol 2016;2:e05.
Schiffl H. Cell cycle arrest biomarkers for the early prediction of acute kidney injury – Full of promise, but not a must-have for yet. J Renal Inj Prev 2017;6:177-83.
Asadi-Samani M, Nasrollah N, Bahmani M. A report of the most important medicinal plants with anti-angiogenesis effects. Angiol Persica Acta 2016;1:e10.
Afkhami-Ardakani M, Hassanzadeh S, Shahrooz R, Asadi-Samani M, Latifi M, Luther T. Phytotherapy and phytopharmacology for reduction of cyclophosphamide-induced toxicity in the male urinary system. J Renal Inj Prev 2017;6:164-70.
Mense ES, Smit AA, Crul M, Franssen EJ. The effect of rapid infusion of cisplatin on nephrotoxicity in patients with lung carcinoma. J Clin Pharm Ther 2019;44:249-57.
Florea AM, Büsselberg D. Cisplatin as an anti-tumor drug: Cellular mechanisms of activity, drug resistance and induced side effects. Cancers (Basel) 2011;3:1351-71.
Altena R, de Haas EC, Nuver J, Brouwer CA, van den Berg MP, Smit AJ, et al.
Evaluation of sub-acute changes in cardiac function after cisplatin-based combination chemotherapy for testicular cancer. Br J Cancer 2009;100:1861-6.
Brozovic A, Ambriović-Ristov A, Osmak M. The relationship between cisplatin-induced reactive oxygen species, glutathione, and BCL-2 and resistance to cisplatin. Crit Rev Toxicol 2010;40:347-59.
Satoh M, Kashihara N, Fujimoto S, Horike H, Tokura T, Namikoshi T, et al.
Anovel free radical scavenger, edarabone, protects against cisplatin-induced acute renal damagein vitro
and in vivo
. J Pharmacol Exp Ther 2003;305:1183-90.
Tamadon MR, Bahadoram M, Zarghami A, Bahadoram S. Administration of N-acetylcysteine for contrast-induced acute kidney injury; new concepts. J Ischemia Tissue Repair 2017;1:e04.
Nasri H. Help or hindrance; administration of herbal drugs for kidney diseases. Toxicol Persa 2016;1:e04.
Crona DJ, Faso A, Nishijima TF, McGraw KA, Galsky MD, Milowsky MI. A systematic review of strategies to prevent cisplatin-induced nephrotoxicity. Oncologist 2017;22:609-19.
Yang Y, Fu Y, Wang P, Liu S, Sha Y, Zhang Y, et al
. Intervention of mitochondrial activity attenuates cisplatin-induced acute kidney injury. Int Urol Nephrol 2019. doi: 10.1007/s11255-019-02113-5.
Mahmoodnia L, Mohammadi K, Masumi R. Ameliorative effect of lycopene effect on cisplatin-induced nephropathy in patient. J Nephropathol 2017;6:144-9.
Quintanilha JCF, Visacri MB, Sousa VM, Bastos LB, Vaz CO, Guarnieri JPO, et al.
Cisplatin-induced human peripheral blood mononuclear cells' oxidative stress and nephrotoxicity in head and neck cancer patients: The influence of hydrogen peroxide. Mol Cell Biochem 2018;440:139-45.
Oh GS, Kim HJ, Shen A, Lee SB, Yang SH, Shim H, et al.
New therapeutic concept of NAD redox balance for cisplatin nephrotoxicity. Biomed Res Int 2016;2016:4048390.
Barnett LMA, Cummings BS. Nephrotoxicity and renal pathophysiology: A contemporary perspective. Toxicol Sci 2018;164:379-90.
Arany I, Sa firstein RL. Cisplatin nephrotoxicity. Semin Nephrol 2003;23:460-4.
Berns JS, Ford PA. Renal toxicities of antineoplastic drugs and bone marrow transplantation. Semin Nephrol 1997;17:54-66.
Taguchi T, Nazneen A, Abid MR, Razzaque MS. Cisplatin-associated nephrotoxicity and pathological events. Contrib Nephrol 2005;148:107-21.
Nasri H. The role of biomarkers in diagnosis of acute kidney injury. Toxicol Persa 2016;1:e03.
Hasanvand A. Ischemia and post-injury regeneration in proximal convoluted tubule cells. Acta Persica Pathophysiol 2017;2:e01.
Rafieian-Kopaei M, Hosseini M, Shirzad H. Comment on: effect of pomegranate flower extract on cisplatin-induced nephrotoxicity in rats. J Nephropathol 2014;3:121-3.
Ridzuan NR, Rashid NA, Othman F, Budin SB, Hussan F, Teoh SL. Protective role of natural products in cisplatin-induced nephrotoxicity. Mini Rev Med Chem 2019. doi: 10.2174/1389557519666190320124438.
Khodadadi S, Rafieian-Kopaei M. Herbs, health and hazards; a nephrology viewpoint on current concepts and new trends. Ann Res Antioxid 2016;1:e05.
Rafieian-Kopaei M, Baradaran A, Rafieian M. Plants antioxidants: From laboratory to clinic. J Nephropathol 2013;2:152-3.
Asgari A. Herbal medicines and kidney; friends or foes? J Nephropharmacol 2014;3:5-6.
Jafari T. Antioxidants; helpful or harmful? Ann Res Antioxid 2016;1:e13.
Shi M, McMillan KL, Wu J, Gillings N, Flores B, Moe OW, et al
. Cisplatin nephrotoxicity as a model of chronic kidney disease. Lab Invest 2018;98:1105-21.
Hajian S. Positive effect of antioxidants on immune system. Immunopathol Persa 2015;1:e02.
Nasri H. Trends toward amelioration of renal inflammation and fibrosis in various kidney diseases. J Inj Inflamm 2016;1:e02.
Nasri H. Herbal drugs and new concepts on its use. J Prev Epidemiol 2016;1:e01.
Hasanvand A, Saberi S. Renin angiotensin system and different mediators induce renal fibrosis. J Ren Endocrinol 2018;4:e09.
Guo Y, Wang M, Mou J, Zhao Z, Yang J, Zhu F, et al.
Pretreatment of Huaiqihuang extractum protects against cisplatin-induced nephrotoxicity. Sci Rep 2018;8:7333.
Baradaran A. Administration of herbal drugs in geriatric individuals; trends on its helps and hazards. Geriatr Persia 2017;1:e01.
Rao M, Praveen Rao PN, Kamath R, Rao MN. Reduction of cisplatin-induced nephrotoxicity by cystone, a polyherbal ayurvedic preparation, in C57BL/6J mice bearing B16F1 melanoma without reducing its antitumor activity. J Ethnopharmacol 1999;68:77-81.
El-Ghiaty MA, Ibrahim OM, Abdou SM, Hussein FZ. Evaluation of the protective effect of Cystone® against cisplatin-induced nephrotoxicity in cancer patients, and its influence on cisplatin antitumor activity. Int Urol Nephrol 2014;46:1367-73.
Sreedevi A, Bharathi K, Prasad KV. Effect of Vernonia cinerea
aerial parts against cisplatin-induced nephrotoxicity in rats. Pharmacol Online 2011;2:548-55.
Qumre Alam, Vijayanarayana K. Nephroprotective effect of alcoholic extracts of fruits of Solanum xanthocarpum
against cisplatin-induced nephrotoxicity in rats. IJAPBC 2013;2:147-51.
Joy J, Nair CK. Amelioration of cisplatin induced nephrotoxicity in Swiss albino
mice by Rubia cordifolia
extract. J Cancer Res Ther 2008;4:111-5.
Iguchi T, Nishikawa M, Chang B, Muroya O, Sato EF, Nakatani T, et al.
Edaravone inhibits acute renal injury and cyst formation in cisplatin-treated rat kidney. Free Radic Res 2004;38:333-41.
Pani SR, Mishra S, Sahoo S, Panda PK. Nephroprotective effect of Bauhinia variegata
(Linn.) whole stem extract against cisplatin-induced nephropathy in rats. Indian J Pharmacol 2011;43:200-2.
] [Full text]
Jayaramalah KK, Anturlikar SD. Cystone, a well-known herbal formulation, inhibits struvite crystal growth formation in single diffusion gel growth technique. J Exp Integr Med 2013;3:51-5.
Baradaran A, Tavafi M, Ardalan MR, Rafieian-Kopaei M. Cisplatin; nephrotoxicity and beyond. Ann Res Antioxid 2016;1:e014.
Nasri H. Trends toward amelioration of cisplatin nephrotoxicity. Ann Res Antioxid 2016;1:e18.
Baradaran A. The role of biomarkers to detect progression of diseases. J Negat Results Clin Exp Stud 2018;1:e05.
Nasri H. On the occasion of world cancer day 2018; breast cancer in geriatric individuals. J Negat Results Clin Exp Stud 2018;1:e03.
Mahmoudian-Sani MR, Mehri-Ghahfarrokhi A, Shojaeian A, Asadi-Samani M, Luther T. The role of microRNAs in human cancers. Immunopathol Persa 2018;4:e05.
Dehghan Shahreza F. Oxidative stress, free radicals, kidney disease and plant antioxidants. Immunopathol Persa 2017;3:11.
Manohar S, Leung N. Cisplatin nephrotoxicity: A review of the literature. J Nephrol 2018;31:15-25.
Miller RP, Tadagavadi RK, Ramesh G, Reeves WB. Mechanisms of cisplatin nephrotoxicity. Toxins (Basel) 2010;2:2490-518.
Tezcan S, Izzettin FV, Sancar M, Yumuk PF, Turhal S. Nephrotoxicity evaluation in outpatients treated with cisplatin-based chemotherapy using a short hydration method. Pharmacol Pharm 2013;4:296.
Nosheen F, Maseehuz Z, Shahid K, Abid H. Detection of early cisplatin induced nephrotoxicity by serial estimation of glomerular filtration rate: Comparison of various methods. Nephro Urol Mon 2010;2:422-30.
Schrier RW. Cancer therapy and renal injury. J Clin Invest 2002;110:743-5.
Zhang JG, Lindup WE. Cisplatin nephrotoxicity: Decreases in mitochondrial protein sulphydryl concentration and calcium uptake by mitochondria from rat renal cortical slices. Biochem Pharmacol 1994;47:1127-35.
Mistry P, Merazga Y, Spargo DJ, Riley PA, McBrien DC. The effects of cisplatin on the concentration of protein thiols and glutathione in the rat kidney. Cancer Chemother Pharmacol 1991;28:277-82.
Matsushima H, Yonemura K, Ohishi K, Hishida A. The role of oxygen free radicals in cisplatin-induced acute renal failure in rats. J Lab Clin Med 1998;131:518-26.
Ali BH, Al Moundhri MS. Agents ameliorating or augmenting the nephrotoxicity of cisplatin and other platinum compounds: A review of some recent research. Food Chem Toxicol 2006;44:1173-83.
Appenroth D, Winnefeld K, Schröter H, Rost M. Beneficial effect of acetylcysteine on cisplatin nephrotoxicity in rats. J Appl Toxicol 1993;13:189-92.
Kheradmand A, Alirezaei M, Asadian P, Rafiei Alavi E, Joorabi S. Antioxidant enzyme activity and MDA level in the rat testis following chronic administration of ghrelin. Andrologia 2009;41:335-40.
Lagrange JL, Médecin B, Etienne MC, Pivot X, Cassuto-Viguier E, Renée N, et al.
Cisplatin nephrotoxicity: A multivariate analysis of potential predisposing factors. Pharmacotherapy 1997;17:1246-53.
Cubillo A, Cornide M, López JL, Molina R, Feliu J, Espinosa E, et al.
Renal tolerance to cisplatin in patients 70 years and older. Am J Clin Oncol 2001;24:192-7.
de Jongh FE, van Veen RN, Veltman SJ, de Wit R, van der Burg ME, van den Bent MJ, et al.
Weekly high-dose cisplatin is a feasible treatment option: Analysis on prognostic factors for toxicity in 400 patients. Br J Cancer 2003;88:1199-206.
[Table 1], [Table 2]