AI Article Synopsis

  • Activin B, a member of the TGF-β family, is overexpressed in oral squamous cell carcinoma (OSCC) and correlates with lymph node metastasis.
  • Research showed that reducing INHBB expression in OSCC cells decreased their invasiveness and migration, but adding activin B restored these abilities.
  • Findings suggest that activin B influences the epithelial-mesenchymal transition (EMT) process in OSCC, indicating its potential as a biomarker for predicting metastasis in this type of cancer.

Article Abstract

Activin B, a homodimer of inhibin beta b (INHBB), is a multifunctional cytokine belonging to the transforming growth factor-β (TGF-β) family. However, the molecular functions and clinical relevance of activin B have not been determined in oral cancer. We investigated the critical roles of activin B in oral squamous cell carcinoma (OSCC). We performed quantitative reverse transcriptase-polymerase chain reaction, Western blotting, and immunohistochemistry to study INHBB expression in OSCC-derived cell lines and OSCC clinical samples. The INHBB expression levels were significantly (P < 0.05) overexpressed in OSCCs compared to normal counterparts and . Activin B-positivity in OSCC cases was significantly (P < 0.05) correlated with regional lymph node metastasis. The INHBB knockdown (shINHBB) cells promoted cellular adhesion and suppression of cellular invasiveness and migration. After treatment of shINHBB cells with activin B, those activities were restored similar to the shMock cells. In the processes of invasiveness and metastasis, the cells cause epithelial-mesenchymal transition (EMT). TGF-β and its family members are promoters of the EMT process. To investigate whether activin B is related to EMT, we examined the expressions of EMT-related genes and found that INHBB was related closely to EMT. Our results suggested for the first time that activin B indicates tumoral metastasis in OSCCs and might be a useful biomarker for OSCC metastasis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559965PMC
http://dx.doi.org/10.7150/jca.18714DOI Listing

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