Personalized medicine for targeted and platinum-based chemotherapy of lung and bladder cancer

被引:2
|
作者
Cimino, George D. [1 ]
Pan, Chong-xian [2 ,3 ,4 ]
Henderson, Paul T. [1 ,2 ,3 ]
机构
[1] Accelerated Med Diagnost Inc, Davis, CA 95618 USA
[2] Univ Calif Davis, Dept Internal Med, Div Hematol & Oncol, Sacramento, CA 94568 USA
[3] UC Davis Comprehens Canc Ctr, Sacramento, CA 94568 USA
[4] VA Northern Calif Hlth Care Syst, Hematol Oncol, Mather, CA 95655 USA
基金
美国国家科学基金会;
关键词
DNA-ADDUCT FORMATION; FACTOR RECEPTOR GENE; PATIENTS RECEIVING CISPLATIN; INTRAPATIENT DOSE-ESCALATION; MASS-SPECTROMETRIC ANALYSIS; POLYMERASE-CHAIN-REACTION; MESSENGER-RNA EXPRESSION; PROSPECTIVE PHASE-II; EGFR MUTATIONS; OVARIAN-CANCER;
D O I
10.4155/BIO.12.325
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The personalized medicine revolution is occurring for cancer chemotherapy. Biomarkers are increasingly capable of distinguishing genotypic or phenotypic traits of individual tumors, and are being linked to the selection of treatment protocols. This review covers the molecular basis for biomarkers of response to targeted and cytotoxic lung and bladder cancer treatment with an emphasis on platinum-based chemotherapy. Platinum derivatives are a class of drugs commonly employed against solid tumors that kill cells by covalent attachment to DNA. Platinum-DNA adduct levels in patient tissues have been correlated to response and survival. The sensitivity and precision of adduct detection has increased to the point of enabling subtherapeutic dosing for diagnostics applications, termed diagnostic microdosing, prior to the initiation of full-dose therapy. The clinical status of this unique phenotypic marker for lung and bladder cancer applications is detailed along with discussion of future applications.
引用
收藏
页码:369 / 391
页数:23
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