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

Identifieur interne : 001331 ( Main/Exploration ); précédent : 001330; suivant : 001332

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

Auteurs : Guang-Ang Tian ; Chun-Chao Zhu ; Xiao-Xin Zhang ; Lei Zhu ; Xiao-Mei Yang ; Shu-Heng Jiang ; Rong-Kun Li ; Lin Tu ; Yang Wang ; Chun Zhuang ; Ping He ; Qing Li ; Xiao-Yan Cao ; Hui Cao ; Zhi-Gang Zhang

Source :

RBID : PMC:4978997

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.


Url:
DOI: 10.1038/srep31071
PubMed: 27506146
PubMed Central: 4978997


Affiliations:


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Le document en format XML

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<name sortKey="Li, Rong Kun" sort="Li, Rong Kun" uniqKey="Li R" first="Rong-Kun" last="Li">Rong-Kun Li</name>
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<name sortKey="Tu, Lin" sort="Tu, Lin" uniqKey="Tu L" first="Lin" last="Tu">Lin Tu</name>
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<name sortKey="Wang, Yang" sort="Wang, Yang" uniqKey="Wang Y" first="Yang" last="Wang">Yang Wang</name>
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<name sortKey="Zhuang, Chun" sort="Zhuang, Chun" uniqKey="Zhuang C" first="Chun" last="Zhuang">Chun Zhuang</name>
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</nlm:aff>
<wicri:noCountry code="nlm country">P.R. China</wicri:noCountry>
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<author>
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</nlm:aff>
<wicri:noCountry code="nlm country">P.R. China</wicri:noCountry>
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<front>
<div type="abstract" xml:lang="en">
<p>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.
<italic>In vitro</italic>
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.</p>
</div>
</front>
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