AI Article Synopsis

  • The study investigates how homotypic cell-in-cell (hoCIC) structures are linked to tumor development, focusing on the role of Protocadherin-7 (PCDH7).
  • PCDH7 is revealed to negatively regulate hoCIC formation through its control over intercellular adhesion and actomyosin dynamics.
  • The research uncovers that PCDH7 promotes tumor growth by inhibiting hoCIC structures via interaction with the protein phosphatase PP1α.

Article Abstract

Though homotypic cell-in-cell (hoCIC) structures are implicated in the development and progression of multiple human tumors, the molecular mechanisms underlying their formation remain poorly understood. We found that the expression of Protocadherin-7 (PCDH7), an integral membrane protein, was negatively associated with the formation of hoCIC structures. Overexpression of efficiently inhibits, while its depletion significantly enhances, hoCIC formation, which was attributed to its regulation on intercellular adhesion and contractile actomyosin as well. Via directly interacting with and inactivating PP1α, a protein phosphatase that dephosphorylates pMLC2, PCDH7 increases the level of pMLC2 leading to enhanced actomyosin at the intercellular region and compromised hoCIC formation. Remarkably, enhanced anchorage-independent cell growth in a hoCIC-dependent manner. Together, we identified PCDH7 as the first membrane protein that inhibits hoCIC formation to promote tumor growth.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7225324PMC
http://dx.doi.org/10.3389/fcell.2020.00329DOI Listing

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