Pharmacogenomics of cisplatin-induced ototoxicity

被引:1
作者
Mukherjea, Debashree [1 ]
Rybak, Leonard P. [1 ]
机构
[1] So Illinois Univ, Sch Med, Dept Surg, Div Otolaryngol, Springfield, IL 62794 USA
基金
美国国家卫生研究院;
关键词
audiometry; cisplatin; COMT; genome-wide screening; glutathione; GST; GSTM1; GSTP1; megalin; ototoxicity; pharmacogenomics; SNP; TMPT; XPC; GLUTATHIONE-S-TRANSFERASE; TRANS-STILBENE OXIDE; GENETIC-VARIANTS; INDIVIDUAL SENSITIVITY; HETEROLOGOUS EXPRESSION; INDUCED CYTOTOXICITY; RECEIVING CISPLATIN; MOLECULAR-CLONING; T1; POLYMORPHISMS; HEARING-LOSS;
D O I
10.2217/PGS.11.48
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cisplatin ototoxicity affects different individuals in a widely variable manner. These variations are likely to be explained by genetic differences among those affected. It would be highly advantageous to identify genetic variants that predispose to cisplatin ototoxicity in order to minimize the risk to susceptible subgroups. Although this area of research is very important, only a few studies have rigorously examined the genetic basis for cisplatin-induced susceptibility to hearing loss. This article addresses recent progress in clarifying the incidence of cisplatin ototoxicity and the risk factors and controversies regarding the identification of genetic variants associated with cisplatin-induced hearing loss.
引用
收藏
页码:1039 / 1050
页数:12
相关论文
共 81 条
  • [1] Regulation of JNK signaling by GSTp
    Adler, V
    Yin, ZM
    Fuchs, SY
    Benezra, M
    Rosario, L
    Tew, KD
    Pincus, MR
    Sardana, M
    Henderson, CJ
    Wolf, CR
    Davis, RJ
    Ronai, Z
    [J]. EMBO JOURNAL, 1999, 18 (05) : 1321 - 1334
  • [2] Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans
    Ahmed, Zubair M.
    Masmoudi, Saber
    Kalay, Ersan
    Belyantseva, Inna A.
    Mosrati, Mohamed Ali
    Collin, Rob W. J.
    Riazuddin, Saima
    Hmani-Aifa, Mounira
    Venselaar, Hanka
    Kawar, Mayya N.
    Tlili, Abdelaziz
    van der Zwaag, Bert
    Khan, Shahid Y.
    Ayadi, Leila
    Riazuddin, S. Amer
    Morell, Robert J.
    Griffith, Andrew J.
    Charfedine, Ilhem
    Caylan, Refik
    Oostrik, Jaap
    Karaguzel, Ahmet
    Ghorbel, Abdelmonem
    Riazuddin, Sheikh
    Friedman, Thomas B.
    Ayadi, Hammadi
    Kremer, Hannie
    [J]. NATURE GENETICS, 2008, 40 (11) : 1335 - 1340
  • [3] AliOsman F, 1997, J BIOL CHEM, V272, P10004
  • [4] [Anonymous], PROTEIN KNOWLEDGEBAS
  • [5] [Anonymous], Drug Metabolism
  • [6] A multiplex polymerase chain reaction protocol for the simultaneous analysis of the glutathione S-transferase GSTM1 and GSTT1 polymorphisms
    Arand, M
    Muhlbauer, R
    Hengstler, J
    Jager, E
    Fuchs, J
    Winkler, L
    Oesch, F
    [J]. ANALYTICAL BIOCHEMISTRY, 1996, 236 (01) : 184 - 186
  • [7] Ban N, 1996, CANCER RES, V56, P3577
  • [8] Glutathione S-transferase M1 and T1 polymorphisms may predict adverse effects after therapy in children with medulloblastoma
    Barahmani, Nadia
    Carpentieri, Sarah
    Li, Xio-Nan
    Wang, Tao
    Cao, Yumei
    Howe, Laura
    Kilburn, Lindsay
    Chintagumpala, Murali
    Lau, Ching
    Okcu, M. Fatih
    [J]. NEURO-ONCOLOGY, 2009, 11 (03) : 292 - 300
  • [9] Platinum compound-related ototoxicity in children - Long-term follow-up reveals continuous worsening of hearing loss
    Bertolini, P
    Lassalle, M
    Mercier, G
    Raquin, MA
    Izzi, G
    Corradini, N
    Hartmann, O
    [J]. JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 2004, 26 (10) : 649 - 655
  • [10] GENETIC-HETEROGENEITY OF THE HUMAN GLUTATHIONE TRANSFERASES - A COMPLEX OF GENE FAMILIES
    BOARD, P
    COGGAN, M
    JOHNSTON, P
    ROSS, V
    SUZUKI, T
    WEBB, G
    [J]. PHARMACOLOGY & THERAPEUTICS, 1990, 48 (03) : 357 - 369