Polymorphisms in solute carrier genes (SLC19A1, SLCO1B1, and SLCO1B3) predicts survival and toxicity in North Indian lung cancer patients undergoing platinum-based doublet chemotherapy

被引:2
|
作者
Sharma, Parul [1 ]
Singh, Navneet [2 ]
Sharma, Siddharth [1 ]
机构
[1] Thapar Inst Engn & Technol, Dept Biotechnol, Patiala, Punjab, India
[2] Post Grad Inst Med Educ & Res, Dept Pulm Med, Chandigarh, India
关键词
lung carcinoma; overall survival; platinum-based doublet chemotherapy; polymorphism; SLC transporters; toxicity; TRANSPORTING POLYPEPTIDE 1B1; DRUG DISPOSITION; OATP-C; METHOTREXATE; ASSOCIATION; POPULATION; RISK; PHARMACOGENETICS; EXPRESSION; VARIANTS;
D O I
10.1111/jcpt.13748
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
What is Known and Objective Solute Carrier (SLC) transporters are known mediators of drug disposition that facilitate the influx of substrates and various chemotherapeutic agents into cells. Polymorphisms in the SLC19A1, SLCO1B1, and SLCO1B3 gene influence the prognosis in the cancer patients, but little is known about their role in lung cancer in Asians. So, the current study aims to investigate the polymorphisms in SLC19A1, SLCO1B1, and SLCO1B3 genes in Northern Indian lung cancer patients. Methods Patients with lung cancer who had a confirmed histology and cytology diagnosis were enrolled in the study. SLC polymorphisms were assessed by Polymerase Chain Reaction-Restriction Fragment Length Polymorphism (PCR-RFLP) for variations in SLC19A1 (G(80)A), SLCO1B1 (A(388)G, (TC)-C-521), and SLCO1B3 (A(1683-5676)G). Results and Discussion Our results showed that mutant genotype for SLC19A1 G(80)A polymorphism had higher median survival time (MST) compared to wild genotype. ADCC patients with mutant genotype showed better survival compared to wild genotype for SLC19A1 G(80)A. SCLC patients G(80)A polymorphism showed increased survival in patients with mutant genotype (p = 0.04). In SLCO1B3, A(1683-5676)G patients carrying heterozygous alleles and administered with platinum and docetaxel showed inferior survival (p = 0.006). In (TC)-C-521 variant, patients with carrier genotype had reduced chances of developing anaemia (p = 0.04). Patients with SLC19A1 and SLCO1B3 variants showed lower incidence of thrombocytopenia and nephrotoxicity. What is New and Conclusion Our findings imply that Solute Carrier gene polymorphisms modulate the overall survival in lung cancer patients undergoing platin-based doublet chemotherapy, also these polymorphisms have a modifying impact on the associated adverse events/toxicity.
引用
收藏
页码:2049 / 2067
页数:19
相关论文
共 50 条
  • [21] Expression of SLCO Transport Genes in Castration-Resistant Prostate Cancer and Impact of Genetic Variation in SLCO1B3 and SLCO2B1 on Prostate Cancer Outcomes
    Wright, Jonathan L.
    Kwon, Erika M.
    Ostrander, Elaine A.
    Montgomery, R. Bruce
    Lin, Daniel W.
    Vessella, Robert
    Stanford, Janet L.
    Mostaghel, Elahe A.
    CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2011, 20 (04) : 619 - 627
  • [22] Prolonged neutropenia after irinotecan-based chemotherapy in a child with polymorphisms of UGT1A1 and SLCO1B1
    Sakaguchi, S.
    Garcia-Bournissen, F.
    Kim, R.
    Schwarz, U. I.
    Nathan, P. C.
    Ito, S.
    ARCHIVES OF DISEASE IN CHILDHOOD, 2009, 94 (12) : 981 - 982
  • [23] THE INFLUENCE OF SLCO1B3 POLYMORPHISMS ON DOCETAXEL DISPOSITION IN ASIAN NASOPHARYNGEAL CARCINOMA PATIENTS
    Chew, S.
    Mann, O.
    Ramasamy, R.
    Lim, W.
    Tan, E.
    Lee, E. J.
    Chowbay, B.
    ANNALS OF ONCOLOGY, 2010, 21 : 52 - 52
  • [24] NOVEL AND REPLICATED GENETIC PREDICTORS FOR NEPHROTOXICITY AND DELAYED METHOTREXATE CLEARANCE: NATIVE AMERICAN ANCESTRY AND THE GENES SLCO1B1, SLC19A1, ABCC4
    Zobeck, Mark
    Bernhardt, Melanie
    Rabin, Karen
    Kamdar, Kala
    Lupo, Philip
    Scheurer, Michael
    PEDIATRIC BLOOD & CANCER, 2022, 69
  • [25] SLCO2B1 and SLCO1B3 May Determine Time to Progression for Patients Receiving Androgen Deprivation Therapy for Prostate Cancer
    Yang, Ming
    Xie, Wanling
    Mostaghel, Elahe
    Nakabayashi, Mari
    Werner, Lillian
    Sun, Tong
    Pomerantz, Mark
    Freedman, Matthew
    Ross, Robert
    Regan, Meredith
    Sharifi, Nima
    Figg, William Douglas
    Balk, Steven
    Brown, Myles
    Taplin, Mary-Ellen
    Oh, William K.
    Lee, Gwo-Shu Mary
    Kantoff, Philip W.
    JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (18) : 2565 - 2573
  • [26] Genetic Polymorphisms in SLCO1B3 and SLCO2B1 May Influence the Racial Difference in the Response to Androgen Deprivation Therapy in Advanced Prostate Cancer
    Fujimoto, N.
    Kubo, T.
    Inatomi, H.
    Hoai, B.
    Yoshida, T.
    Shiota, M.
    Matsumoto, T.
    UROLOGY, 2012, 80 (03) : S80 - S80
  • [27] Association of SLCO1B1 gene polymorphisms with toxicity response of high dose methotrexate chemotherapy in childhood acute lymphoblastic leukemia
    Li, Jun
    Wang, Xiao-Ru
    Zhai, Xiao-Wen
    Wang, Hong-Sheng
    Qian, Xiao-Wen
    Miao, Hui
    Zhu, Xiao-Hua
    INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE, 2015, 8 (04): : 6109 - 6113
  • [28] Severe toxicities after irinotecan-based chemotherapy in a patient with lung cancer: A homozygote for the SLCO1B1*15 allele
    Takane, Hiroshi
    Miyata, Masanori
    Burioka, Naoto
    Kurai, Jun
    Fukuoka, Yasushi
    Suyama, Hisashi
    Shigeoka, Yasushi
    Otsubo, Kenji
    Ieiri, Ichiro
    Shimizu, Eiji
    THERAPEUTIC DRUG MONITORING, 2007, 29 (05) : 666 - 668
  • [29] Impact of SLCO1B3 polymorphisms on clinical outcomes in lung allograft recipients receiving mycophenolic acid
    Laneshia K. Tague
    Derek E. Byers
    Ramsey Hachem
    Daniel Kreisel
    Alexander S. Krupnick
    Hrishikesh S. Kulkarni
    Catherine Chen
    Howard J. Huang
    Andrew Gelman
    The Pharmacogenomics Journal, 2020, 20 : 69 - 79
  • [30] Impact of SLCO1B3 polymorphisms on clinical outcomes in lung allograft recipients receiving mycophenolic acid
    Tague, Laneshia K.
    Byers, Derek E.
    Hachem, Ramsey
    Kreisel, Daniel
    Krupnick, Alexander S.
    Kulkarni, Hrishikesh S.
    Chen, Catherine
    Huang, Howard J.
    Gelman, Andrew
    PHARMACOGENOMICS JOURNAL, 2020, 20 (01): : 69 - 79