Association of ABCB1 and SLC22A16 Gene Polymorphisms with Incidence of Doxorubicin-Induced Febrile Neutropenia: A Survey of Iranian Breast Cancer Patients

被引:20
作者
Faraji, Abolfazl [1 ]
Manshadi, Hamid Reza Dehghan [2 ]
Mobaraki, Maryam [1 ]
Zare, Mahkameh [2 ]
Houshmand, Massoud [1 ]
机构
[1] Natl Inst Genet Engn & Biotechnol, Dept Med Genet, Tehran, Iran
[2] Iran Univ Med Sci, Dept Radiat Oncol, Tir Hosp 7, Tehran, Iran
来源
PLOS ONE | 2016年 / 11卷 / 12期
关键词
CHEMOTHERAPY; DOCETAXEL;
D O I
10.1371/journal.pone.0168519
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Breast cancer is the most common cancer in women worldwide. Doxorubicin-based chemotherapy is used to treat breast cancer patients; however, neutropenia is a common hematologic side effect and can be life-threatening. The ABCB1 and SLC22A16 genes encode proteins that are essential for doxorubicin transport. In this study, we explored the effect of 2 common polymorphisms in ABCB1 (rs10276036 C/T) and SLC22A16 (rs12210538 A/G) on the development of grade 3/4 febrile neutropenia in Iranian breast cancer patients. Our results showed no significant association between these polymorphisms and grade 3/4 febrile neutropenia; however, allele C of ABCB1 (rs10276036 C/T) (p = 0.315, OR = 1.500, 95% CI = 0.679-3.312) and allele A of SLC22A16 (rs12210538 A/G) (p = 0.110, OR= 2.984, 95% CI = 0.743-11.988) tended to have a greater association with grade 3/4 febrile neutropenia, whereas allele T of ABCB1 (rs10276036) (p = 0.130, OR = 0.515, 95% CI = 0.217-1.223) and allele G of SLC22A16 (rs12210538) (p = 0.548, OR = 0.786, 95% CI = 0.358-1.726) tended to protect against this condition. In addition to breast cancer, a statistically significant association was also observed between the development of grade 3/4 febrile neutropenia and other clinical manifestations such as stage IIIC cancer (p = 0.037) and other diseases (p = 0.026). Our results indicate that evaluation of the risk of grade 3/4 neutropenia development and consideration of molecular and clinical findings may be of value when screening for high-risk breast cancer patients.
引用
收藏
页数:10
相关论文
共 26 条
  • [1] [Anonymous], 1986, P NATL ACAD SCI US, V83, P4514
  • [2] [Anonymous], 1993, PHARM THER, V60, P185
  • [3] [Anonymous], 2007, PHARMACOGENOMICS, V8, P567, DOI [10.2217/14622416.8.6.567, DOI 10.2217/14622416.8.6.567]
  • [4] [Anonymous], 2007, INT J GYNECOL PATHOL, V26, P334, DOI [10.1097/01.pgp.0000236951.33914.1b, DOI 10.1097/01.PGP.0000236951.33914.1B]
  • [5] [Anonymous], 1997, J BIOL CHEM, V272, P10685
  • [6] [Anonymous], 2015, CANCER CHEMOTH PHARM, V75, P207, DOI [10.1007/s00280-014-2632-4, DOI 10.1007/S00280-014-2632-4]
  • [7] [Anonymous], 1987, CANC RES, V47, P5141
  • [8] [Anonymous], 2010, BRIT J CANCER, V102, P1003, DOI [10.1038/sj.bjc.6605587, DOI 10.1038/SJ.BJC.6605587]
  • [9] [Anonymous], 1998, CLIN CANC RES, V4, P389
  • [10] [Anonymous], 2014, CRIT REV ONCOL HEMAT, V90, P190, DOI [10.1016/j.critrevonc.2013.12.006, DOI 10.1016/J.CRITREVONC.2013.12.006]