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CADM1 promotes malignant features of small-cell lung cancer by recruiting 4.1R to the plasma membrane.
Funaki, Toko; Ito, Takeshi; Tanei, Zen-Ichi; Goto, Akiteru; Niki, Toshiro; Matsubara, Daisuke; Murakami, Yoshinori.
Afiliación
  • Funaki T; Division of Molecular Pathology, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
  • Ito T; Division of Molecular Pathology, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
  • Tanei ZI; Department of Cancer Pathology, Faculty of Medicine, Hokkaido University, Sapporo, Japan.
  • Goto A; Department of Cellular and Organ Pathology, Graduate School of Medicine, Akita University, Akita, Japan.
  • Niki T; Department of Integrative Pathology, Jichi Medical University, Shimotsuke, Japan.
  • Matsubara D; Division of Molecular Pathology, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan; Department of Integrative Pathology, Jichi Medical University, Shimotsuke, Japan.
  • Murakami Y; Division of Molecular Pathology, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan. Electronic address: ymurakam@ims.u-tokyo.ac.jp.
Biochem Biophys Res Commun ; 534: 172-178, 2021 01 01.
Article en En | MEDLINE | ID: mdl-33298314
ABSTRACT
Cell adhesion molecule 1 (CADM1), which mediates intercellular adhesion between epithelial cells, is shown to be highly expressed in small-cell lung cancer (SCLC) and to enhance tumorigenicity of SCLC cells in nude mice. Here, we investigated the molecular mechanism underlying the oncogenic role of CADM1 in SCLC. CADM1 promoted colony formation of SCLC cells in soft agar. Analysis of deletion and point mutants of the conserved protein-binding motifs in CADM1 revealed that the 4.1 protein-binding motif in the cytoplasmic domain is responsible for the promotion of colony formation. Among the actin-binding 4.1 proteins, 4.1R was the only protein whose localization to the plasma membrane is dependent on CADM1 expression in SCLC cells. Knockdown of 4.1R suppressed the colony formation enhanced by CADM1, suggesting that 4.1R is required for the oncogenic role of CADM1 in SCLC. In primary SCLC, CADM1 expression was correlated with membranous localization of 4.1R, as was observed in a SCLC cell line. Moreover, membranous co-localization of CADM1 and 4.1R was associated with more advanced tumor stage. These results suggest that the formation of CADM1-4.1R complex would promote malignant features of SCLC.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteínas del Citoesqueleto / Carcinoma Pulmonar de Células Pequeñas / Molécula 1 de Adhesión Celular / Neoplasias Pulmonares / Proteínas de la Membrana Límite: Animals Idioma: En Revista: Biochem Biophys Res Commun Año: 2021 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteínas del Citoesqueleto / Carcinoma Pulmonar de Células Pequeñas / Molécula 1 de Adhesión Celular / Neoplasias Pulmonares / Proteínas de la Membrana Límite: Animals Idioma: En Revista: Biochem Biophys Res Commun Año: 2021 Tipo del documento: Article País de afiliación: Japón