Literature DB >> 26373844

Identifying therapeutic targets in gastric cancer: the current status and future direction.

Beiqin Yu1, Jingwu Xie2.   

Abstract

Gastric cancer is the third leading cause of cancer-related death worldwide. Our basic understanding of gastric cancer biology falls behind that of many other cancer types. Current standard treatment options for gastric cancer have not changed for the last 20 years. Thus, there is an urgent need to establish novel strategies to treat this deadly cancer. Successful clinical trials with Gleevec in CML and gastrointestinal stromal tumors have set up an example for targeted therapy of cancer. In this review, we will summarize major progress in classification, therapeutic options of gastric cancer. We will also discuss molecular mechanisms for drug resistance in gastric cancer. In addition, we will attempt to propose potential future directions in gastric cancer biology and drug targets.
© The Author 2015. Published by ABBS Editorial Office in association with Oxford University Press on behalf of the Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences.

Entities:  

Keywords:  Wnt; cancer stem cell; gastric cancer; hedgehog; targeted therapy

Mesh:

Substances:

Year:  2015        PMID: 26373844      PMCID: PMC4689156          DOI: 10.1093/abbs/gmv084

Source DB:  PubMed          Journal:  Acta Biochim Biophys Sin (Shanghai)        ISSN: 1672-9145            Impact factor:   3.848


  80 in total

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Journal:  PLoS One       Date:  2013-11-01       Impact factor: 3.240

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2.  Interference of P-REX2a may inhibit proliferation and reverse the resistance of SGC7901 cells to doxorubicin.

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3.  Identification of a novel YAP-14-3-3ζ negative feedback loop in gastric cancer.

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4.  YAP signaling in gastric cancer-derived mesenchymal stem cells is critical for its promoting role in cancer progression.

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5.  GLI1-mediated regulation of side population is responsible for drug resistance in gastric cancer.

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Review 6.  Long non-coding small nucleolar RNA host genes in digestive cancers.

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9.  CDK2 positively regulates aerobic glycolysis by suppressing SIRT5 in gastric cancer.

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  9 in total

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