Clin Cancer Res. 2015;21(2):357-64.
Significant association of oncogene YAP1 with poor prognosis and cetuximab resistance in colorectal cancer patients.
제1저자 이근욱, 이성숙 · 교신저자 이주석
소속 (9)
- Department of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas. Department of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Gyeonggi-do, Korea.
- Department of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas. Department of Hematology-Oncology, Inje University Haeundae Paik Hospital, Busan, Korea.
- Department of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
- Department of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas. Department of Thoracic Surgery, Center for Lung Cancer, Research Institute and Hospital, National Cancer Center, Goyang, Gyeonggi-do, Korea.
- ASAN Institute for Life Sciences, ASAN Medical Center, Department of Medicine, University of Ulsan College of Medicine, Seoul, Korea.
- Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
- Department of Biochemistry and Molecular Biology, Medical Research Center for Bioreaction to Reactive Oxygen Species and Biomedical Science Institute, School of Medicine, Kyung Hee University, Seoul, Korea.
- Division of Hemato-Oncology, Department of Internal Medicine, Korea University Medical Center, Korea University College of Medicine, Seoul, Korea.
- Department of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas. Department of Biochemistry and Molecular Biology, Medical Research Center for Bioreaction to Reactive Oxygen Species and Biomedical Science Institute, School of Medicine, Kyung Hee University, Seoul, Korea. jlee@mdanderson.org.
Abstract
PURPOSE Activation of YAP1, a novel oncogene in the Hippo pathway, has been observed in many cancers, including colorectal cancer. We investigated whether activation of YAP1 is significantly associated with prognosis or treatment outcomes in colorectal cancer.
EXPERIMENTAL DESIGN A gene expression signature reflecting YAP1 activation was identified in colorectal cancer cells, and patients with colorectal cancer were stratified into two groups according to this signature: activated YAP1 colorectal cancer (AYCC) or inactivated YAP1 colorectal cancer (IYCC). Stratified patients in five test cohorts were evaluated to determine the effect of the signature on colorectal cancer prognosis and response to cetuximab treatment.
RESULTS The activated YAP1 signature was associated with poor prognosis for colorectal cancer in four independent patient cohorts with stage I-III disease (total n = 1,028). In a multivariate analysis, the impact of the YAP1 signature on disease-free survival was independent of other clinical variables [hazard ratio (HR), 1.63; 95% confidence interval (CI), 1.25-2.13; P < 0.001]. In patients with stage IV colorectal cancer and wild-type KRAS, IYCC patients had a better disease control rate and progression-free survival (PFS) after cetuximab monotherapy than did AYCC patients; however, in patients with KRAS mutations, PFS duration after cetuximab monotherapy was not different between IYCC and AYCC patients. In multivariate analysis, the effect of YAP1 activation on PFS was independent of KRAS mutation status and other clinical variables (HR, 1.82; 95% CI, 1.05-3.16; P = 0.03).
CONCLUSIONS Activation of YAP1 is highly associated with poor prognosis for colorectal cancer and may be useful in identifying patients with metastatic colorectal cancer resistant to cetuximab.
©2014 American Association for Cancer Research.
Conflict of interest statement
Disclosure of Potential Conflicts of Interest. No potential conflicts of interest were disclosed.
그 밖의 정보
- 출판 형태
- Journal Article, Research Support, N.I.H., Extramural
- 저널
- Clinical cancer research : an official journal of the American Association for Cancer Research · eISSN 1557-3265
- 전자 출판
- 2014-11-11
- MeSH
- Adaptor Proteins, Signal Transducing / genetics · Antibodies, Monoclonal, Humanized / pharmacology / therapeutic use · Antineoplastic Agents / pharmacology / therapeutic use · Cell Line, Tumor · Cetuximab · Colorectal Neoplasms / drug therapy / genetics / mortality · Disease-Free Survival · Drug Resistance, Neoplasm · Humans · Phosphoproteins / genetics · Prognosis · Transcription Factors · Transcriptome · Treatment Outcome · YAP-Signaling Proteins
- Substances
- Adaptor Proteins, Signal Transducing · Antibodies, Monoclonal, Humanized · Antineoplastic Agents · Phosphoproteins · Transcription Factors · YAP-Signaling Proteins · YAP1 protein, human · Cetuximab
- 연구비
- NCI NIH HHS P30 CA016672 · NCI NIH HHS R01 CA150229 · NCI NIH HHS CA016672 · NCI NIH HHS CA150229
- 참고문헌
- 42편