PLOD2 Is Essential to Functional Activation of Integrin β1 for Invasion/Metastasis in Head and Neck Squamous Cell Carcinomas

Identifying the specific functional regulator of integrin family molecules in cancer cells is critical because they are directly involved in tumor invasion and metastasis. Here we report high expression of PLOD2 in oropharyngeal squamous cell carcinomas (SCCs) and its critical role as a stabilizer o...

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Veröffentlicht in:iScience 2020-02, Vol.23 (2), p.100850-100850, Article 100850
Hauptverfasser: Ueki, Yushi, Saito, Ken, Iioka, Hidekazu, Sakamoto, Izumi, Kanda, Yasuhiro, Sakaguchi, Masakiyo, Horii, Arata, Kondo, Eisaku
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Sprache:eng
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Zusammenfassung:Identifying the specific functional regulator of integrin family molecules in cancer cells is critical because they are directly involved in tumor invasion and metastasis. Here we report high expression of PLOD2 in oropharyngeal squamous cell carcinomas (SCCs) and its critical role as a stabilizer of integrin β1, enabling integrin β1 to initiate tumor invasion/metastasis. Integrin β1 stabilized by PLOD2-mediated hydroxylation was recruited to the plasma membrane, its functional site, and accelerated tumor cell motility, leading to tumor metastasis in vivo, whereas loss of PLOD2 expression abrogated it. In accordance with molecular analysis, examination of oropharyngeal SCC tissues from patients corroborated PLOD2 expression associated with integrin β1 at the invasive front of tumor nests. PLOD2 is thus implicated as the key regulator of integrin β1 that prominently regulates tumor invasion and metastasis, and it provides important clues engendering novel therapeutics for these intractable cancers. [Display omitted] •PLOD2 specifically regulates intracellular localization of integrin β1•The hydroxylation on integrin β1 by PLOD2 is critical for its stability•PLOD2 and integrin β1 expression colocalized at the invasive front of SCC tissues•PLOD2 is necessary for tumor invasion/metastasis through the integrin β1 maturation Molecular Biology; Cancer
ISSN:2589-0042
2589-0042
DOI:10.1016/j.isci.2020.100850