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CCBE1 promotes GIST development through enhancing angiogenesis and mediating resistance to imatinib.


ABSTRACT: Gastrointestinal stromal tumor (GIST) is the most major mesenchymal neoplasm of the digestive tract. Up to now, imatinib mesylate has been used as a standard first-line treatment for irresectable and metastasized GIST patients or adjuvant treatment for advanced GIST patients who received surgical resection. However, secondary resistance to imatinib usually happens, resulting in a major obstacle in GIST successful therapy. In this study, we first found that collagen and calcium binding EGF domains 1 (CCBE1) expression gradually elevated along with the risk degree of NIH classification, and poor prognosis emerged in the CCBE1-positive patients. In vitro experiments showed that recombinant CCBE1 protein can enhance angiogenesis and neutralize partial effect of imatinib on the GIST-T1 cells. In conclusion, these data indicated that CCBE1 may be served as a new predictor of prognosis in post-operative GIST patients and may play an important role in stimulating GIST progression.

SUBMITTER: Tian GA 

PROVIDER: S-EPMC4978997 | biostudies-literature | 2016 Aug

REPOSITORIES: biostudies-literature

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CCBE1 promotes GIST development through enhancing angiogenesis and mediating resistance to imatinib.

Tian Guang-Ang GA   Zhu Chun-Chao CC   Zhang Xiao-Xin XX   Zhu Lei L   Yang Xiao-Mei XM   Jiang Shu-Heng SH   Li Rong-Kun RK   Tu Lin L   Wang Yang Y   Zhuang Chun C   He Ping P   Li Qing Q   Cao Xiao-Yan XY   Cao Hui H   Zhang Zhi-Gang ZG  

Scientific reports 20160810


Gastrointestinal stromal tumor (GIST) is the most major mesenchymal neoplasm of the digestive tract. Up to now, imatinib mesylate has been used as a standard first-line treatment for irresectable and metastasized GIST patients or adjuvant treatment for advanced GIST patients who received surgical resection. However, secondary resistance to imatinib usually happens, resulting in a major obstacle in GIST successful therapy. In this study, we first found that collagen and calcium binding EGF domain  ...[more]

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