A network-based predictive gene-expression signature for adjuvant chemotherapy benefit in stage II colorectal cancer

被引:15
作者
Cao, Bangrong [3 ]
Luo, Liping [3 ]
Feng, Lin [1 ,2 ]
Ma, Shiqi [3 ]
Chen, Tingqing [3 ]
Ren, Yuan [3 ]
Zha, Xiao [3 ]
Cheng, Shujun [1 ,2 ]
Zhang, Kaitai [1 ,2 ]
Chen, Changmin [3 ]
机构
[1] Peking Union Med Coll, Canc Inst & Hosp, Dept Etiol & Carcinogenesis, State Key Lab Mol Oncol, Beijing, Peoples R China
[2] Chinese Acad Med Sci, Beijing, Peoples R China
[3] Univ Elect Sci & Technol China, Sch Med, Sichuan Canc Hosp & Inst, Dept Basic Res,Sichuan Canc Ctr, 55 Renmin Ave,Fourth Sect, Chengdu 610041, Sichuan, Peoples R China
关键词
Colorectal cancer; Biomarkers; Adjuvant chemotherapy; 11-PPI-Mod; B COLON-CANCER; DISEASE PROGRESSION; MOLECULAR MARKERS; MISMATCH REPAIR; CELLS; FLUOROURACIL; HYPOXIA; CARCINOMA; THERAPY; RECURRENCE;
D O I
10.1186/s12885-017-3821-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The clinical benefit of adjuvant chemotherapy for stage II colorectal cancer (CRC) is controversial. This study aimed to explore novel gene signature to predict outcome benefit of postoperative 5-Fu-based therapy in stage II CRC. Methods: Gene-expression profiles of stage II CRCs from two datasets with 5-Fu-based adjuvant chemotherapy (training dataset, n = 212; validation dataset, n = 85) were analyzed to identify the indicator. A systemic approach by integrating gene-expression and protein-protein interaction (PPI) network was implemented to develop the predictive signature. Kaplan-Meier curves and Cox proportional hazards model were used to determine the survival benefit of adjuvant chemotherapy. Experiments with shRNA knock-down were carried out to confirm the signature identified in this study. Results: In the training dataset, we identified 44 PPI sub-modules, by which we separate patients into two clusters (1 and 2) having different chemotherapeutic benefit. A predictor of 11 PPI sub-modules (11-PPI-Mod) was established to discriminate the two sub-groups, with an overall accuracy of 90.1%. This signature was independently validated in an external validation dataset. Kaplan-Meier curves showed an improved outcome for patients who received adjuvant chemotherapy in Cluster 1 sub-group, but even worse survival for those in Cluster 2 sub-group. Similar results were found in both the training and the validation dataset. Multivariate Cox regression revealed an interaction effect between 11-PPI-Mod signature and adjuvant therapy treatment in the training dataset (RFS, p = 0.007; OS, p = 0.006) and the validation dataset (RFS, p = 0.002). From the signature, we found that PTGES gene was up-regulated in CRC cells which were more resistant to 5-Fu. Knock-down of PTGES indicated a growth inhibition and up-regulation of apoptotic markers induced by 5-Fu in CRC cells. Conclusions: Only a small proportion of stage II CRC patients could benefit from adjuvant therapy. The 11-PPI-Mod as a potential predictor could be helpful to distinguish this sub-group with favorable outcome.
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页数:13
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