Spatiotemporal Evolution of the Primary Glioblastoma Genome

Citations

WEB OF SCIENCE

259
Citations

SCOPUS

266

초록

Tumor recurrence following treatment is the major cause of mortality for glioblastoma multiforme (GBM) patients. Thus, insights on the evolutionary process at recurrence are critical for improved patient care. Here, we describe our genomic analyses of the initial and recurrent tumor specimens from each of 38 GBM patients. A substantial divergence in the landscape of driver alterations was associated with distant appearance of a recurrent tumor from the initial tumor, suggesting that the genomic profile of the initial tumor can mislead targeted therapies for the distally recurred tumor. In addition, in contrast to IDH1-mutated gliomas, IDH1-wild-type primary GBMs rarely developed hypermutation following temozolomide (TMZ) treatment, indicating low risk for TMZ-induced hypermutation for these tumors under the standard regimen.

키워드

ACUTE MYELOID-LEUKEMIA; MALIGNANT GLIOMAS; MSH6 MUTATIONS; WHOLE-GENOME; TEMOZOLOMIDE; CANCER; GENES; IDH1; HETEROGENEITY; DNA
제목
Spatiotemporal Evolution of the Primary Glioblastoma Genome
저자
Kim, Jinkuk; Lee, In-Hee; Cho, Hee Jin; Park, Chul-Kee; Jung, Yang-Soon; Kim, Yanghee; Nam, So Hee; Kim, Byung Sup; Johnson, Mark D.; Kong, Doo-Sik; Seol, Ho Jun; Lee, Jung-Il; Joo, Kyeung Min; Yoon, Yeup; Park, Woong-Yang; Lee, Jeongwu; Park, Peter J.; Nam, Do-Hyun
DOI
10.1016/j.ccell.2015.07.013
발행일
2015-09
유형
Article
저널명
Cancer Cell
권
28
호
3
페이지
318 ~ 328