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FBP17-mediated finger-like membrane protrusions in cell competition between normal and RasV12-transformed cells.


ABSTRACT: At the initial stage of carcinogenesis, cell competition often occurs between newly emerging transformed cells and the neighboring normal cells, leading to the elimination of transformed cells from the epithelial layer. For instance, when RasV12-transformed cells are surrounded by normal cells, RasV12 cells are apically extruded from the epithelium. However, the underlying mechanisms of this tumor-suppressive process still remain enigmatic. We first show by electron microscopic analysis that characteristic finger-like membrane protrusions are projected from both normal and RasV12 cells at their interface. In addition, FBP17, a member of the F-BAR proteins, accumulates in RasV12 cells, as well as surrounding normal cells, which plays a positive role in the formation of finger-like protrusions and apical elimination of RasV12 cells. Furthermore, cdc42 acts upstream of these processes. These results suggest that the cdc42/FBP17 pathway is a crucial trigger of cell competition, inducing "protrusion to protrusion response" between normal and RasV12-transformed cells.

SUBMITTER: Kamasaki T 

PROVIDER: S-EPMC8405961 | biostudies-literature | 2021 Sep

REPOSITORIES: biostudies-literature

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FBP17-mediated finger-like membrane protrusions in cell competition between normal and RasV12-transformed cells.

Kamasaki Tomoko T   Miyazaki Yumi Y   Ishikawa Susumu S   Hoshiba Kazuya K   Kuromiya Keisuke K   Tanimura Nobuyuki N   Mori Yusuke Y   Tsutsumi Motosuke M   Nemoto Tomomi T   Uehara Ryota R   Suetsugu Shiro S   Itoh Toshiki T   Fujita Yasuyuki Y  

iScience 20210818 9


At the initial stage of carcinogenesis, cell competition often occurs between newly emerging transformed cells and the neighboring normal cells, leading to the elimination of transformed cells from the epithelial layer. For instance, when RasV12-transformed cells are surrounded by normal cells, RasV12 cells are apically extruded from the epithelium. However, the underlying mechanisms of this tumor-suppressive process still remain enigmatic. We first show by electron microscopic analysis that cha  ...[more]

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