AI Article Synopsis

  • Non-small-cell lung cancer (NSCLC) is commonly diagnosed at an advanced stage, making it crucial to understand the mechanisms behind its metastasis.
  • A study found that high levels of B cell receptor-associated protein 31 (BCAP31) and three other proteins in NSCLC patients were linked to worse survival rates, with BCAP31 being particularly significant.
  • BCAP31 was shown to affect NSCLC cell migration and invasion through the Akt/m-TOR/p70S6K signaling pathway, highlighting its potential as a new prognostic factor and therapeutic target in NSCLC.

Article Abstract

Non-small-cell lung cancer (NSCLC) represents most of lung cancers, is often diagnosed at an advanced metastatic stage. Therefore, exploring the mechanisms underlying metastasis is key to understanding the development of NSCLC. The expression of B cell receptor-associated protein 31 (BCAP31), calreticulin, glucose-regulated protein 78, and glucose-regulated protein 94 were analyzed using immunohistochemical staining of 360 NSCLC patients. It resulted that the high-level expression of the four proteins, but particularly BCAP31, predicted inferior overall survival. What's more, BCAP31 was closely associated with histological grade and p53 status, which was verified by seven cohorts of NSCLC transcript microarray datasets. Then, three NSCLC cell lines were transfected to observe behavior changes BCAP31 caused, we found the fluctuation of BCAP31 significantly influenced the migration, invasion of NSCLC cells. To identify the pathway utilized by BCAP31, Gene Set Enrichment Analysis was firstly performed, showing Akt/m-TOR/p70S6K pathway was the significant one, which was verified by immunofluorescence, kinase phosphorylation and cellular behavioral observations. Finally, the data of label-free mass spectroscopy implied that BCAP31 plays a role in a fundamental biological process. This study provides the first demonstration of BCAP31 as a novel prognostic factor related to metastasis and suggests a new therapeutic strategy for NSCLC.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7055246PMC
http://dx.doi.org/10.1038/s41598-020-60905-7DOI Listing

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