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CCN Family Proteins in Cancer: Insight Into Their Structures and Coordination Role in Tumor Microenvironment

期刊

FRONTIERS IN GENETICS
卷 12, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fgene.2021.649387

关键词

CCN proteins; isoforms; targeted therapy; tumor microenvironment; pan-cancer

资金

  1. National Natural Science Foundation of China [81502694]
  2. Fundamental Research Funds for the Central Universities [1191329835]

向作者/读者索取更多资源

The communication between tumor cells and TME activates signaling pathways that contribute to cancer progression. Targeting multiple components rather than single molecules could be more effective in cancer therapy, with CCN family proteins showing promise. The diverse functions of CCN proteins in different cancers are influenced by the TME and its truncated isoforms, suggesting a potential anti-cancer strategy by targeting CCN proteins to rebalance the TME.
The crosstalk between tumor cells and the tumor microenvironment (TME), triggers a variety of critical signaling pathways and promotes the malignant progression of cancer. The success rate of cancer therapy through targeting single molecule of this crosstalk may be extremely low, whereas co-targeting multiple components could be complicated design and likely to have more side effects. The six members of cellular communication network (CCN) family proteins are scaffolding proteins that may govern the TME, and several studies have shown targeted therapy of CCN family proteins may be effective for the treatment of cancer. CCN protein family shares similar structures, and they mutually reinforce and neutralize each other to serve various roles that are tightly regulated in a spatiotemporal manner by the TME. Here, we review the current knowledge on the structures and roles of CCN proteins in different types of cancer. We also analyze CCN mRNA expression, and reasons for its diverse relationship to prognosis in different cancers. In this review, we conclude that the discrepant functions of CCN proteins in different types of cancer are attributed to diverse TME and CCN truncated isoforms, and speculate that targeting CCN proteins to rebalance the TME could be a potent anti-cancer strategy.

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