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
  • [1] SLCO1B1, SLCO2B1, and SLCO1B3 Polymorphisms and Susceptibility to Bladder Cancer Risk
    Hoai Thi Thu Bui
    Fujimoto, Naohiro
    Kubo, Tatsuhiko
    Inatomi, Hisato
    Matsumoto, Tetsuro
    CANCER INVESTIGATION, 2014, 32 (06) : 256 - 261
  • [2] Ethnic Differences in the Frequency of Polymorphisms in Influx Transporters SLC10A1, SLC22A1, SLCO1B3, and SLCO1B1
    Dias, Vera
    Ribeiro, Vera
    DRUG METABOLISM REVIEWS, 2009, 41 : 77 - 77
  • [3] SLCO1B1 and SLCO1B3 genetic mutations in Taiwanese patients with Rotor syndrome
    Cheng, Ya-Yuan
    Chang, Kai -Chi
    Chen, Pei -Lung
    Yeung, Chun-Yan
    Liou, Bang -Yu
    Chen, Huey -Ling
    JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION, 2023, 122 (07) : 648 - 652
  • [4] Effects of SLCO1B1 and SLCO1B3 Genetic Polymorphisms on Valsartan Pharmacokinetics in Healthy Korean Volunteers
    Song, Gonjin
    Chung, Jee-Eun
    Yee, Jeong
    Lee, Kyung-Eun
    Park, Kyungsoo
    Gwak, Hye-Sun
    JOURNAL OF PERSONALIZED MEDICINE, 2021, 11 (09):
  • [5] UGT1A1, SLCO1B1, and SLCO1B3 polymorphisms vs. neonatal hyperbilirubinemia: is there an association?
    Laura Alencastro de Azevedo
    Themis Reverbel da Silveira
    Clarissa Gutierrez Carvalho
    Simone Martins de Castro
    Roberto Giugliani
    Ursula Matte
    Pediatric Research, 2012, 72 : 169 - 173
  • [6] UGT1A1, SLCO1B1, and SLCO1B3 polymorphisms vs. neonatal hyperbilirubinemia: is there an association?
    de Azevedo, Laura Alencastro
    da Silveire, Themis Reverbel
    Carvalho, Clarissa Gutierrez
    de Castro, Simone Martins
    Giugliani, Roberto
    Matte, Ursula
    PEDIATRIC RESEARCH, 2012, 72 (02) : 169 - 173
  • [7] Comparison of genetic variations of the SLCO1B1, SLCO1B3, and SLCO2B1 genes among five ethnic groups
    Namgoong, Suhg
    Cheong, Hyun Sub
    Kim, Ji On
    Kim, Lyoung Hyo
    Na, Han Sung
    Koh, In Song
    Chung, Myeon Woo
    Shin, Hyoung Doo
    ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY, 2015, 40 (03) : 692 - 697
  • [8] SLC19A1, SLC46A1 and SLCO1B1 Polymorphisms as Predictors of Methotrexate-Related Toxicity in Portuguese Rheumatoid Arthritis Patients
    Lima, Aurea
    Bernardes, Miguel
    Azevedo, Rita
    Monteiro, Joaquim
    Sousa, Hugo
    Medeiros, Rui
    Seabra, Vitor
    TOXICOLOGICAL SCIENCES, 2014, 142 (01) : 196 - 209
  • [9] Influence of Genomic Ancestry on the Distribution of SLCO1B1, SLCO1B3 and ABCB1 Gene Polymorphisms among Brazilians
    Sortica, Vinicius de A.
    Ojopi, Elida B.
    Genro, Julia P.
    Callegari-Jacques, Sidia
    Ribeiro-dos-Santos, Andrea
    de Moraes, Manoel Odorico
    Romano-Silva, Marco A.
    Pena, Sergio D. J.
    Suarez-Kurtz, Guilherme
    Hutz, Mara H.
    BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY, 2012, 110 (05) : 460 - 468
  • [10] CYP2C9, SLCO1B1, SLCO1B3, and ABCB11 Polymorphisms in Patients With Bosentan-Induced Liver Toxicity
    Roustit, M.
    Fonrose, X.
    Montani, D.
    Girerd, B.
    Stanke-Labesque, F.
    Gonnet, N.
    Humbert, M.
    Cracowski, J-L
    CLINICAL PHARMACOLOGY & THERAPEUTICS, 2014, 95 (06) : 583 - 585