AI Article Synopsis

  • Small-cell lung cancer (SCLC) shows increased levels of specific oncogenes like Myc and YAP1 while suppressing tumor suppressor genes.
  • A study compared plasma proteins from 15 newly diagnosed SCLC patients and 15 patients before diagnosis to 30 matched controls, finding 272 proteins elevated in newly diagnosed cases, with some identified a year prior to diagnosis.
  • Analysis revealed key pathways linked to MYC and YAP1, with shared traits found in SCLC cell lines, suggesting new protein markers for early-stage SCLC and highlighting inflammation preceding diagnosis.

Article Abstract

Small-cell-lung cancer (SCLC) is associated with overexpression of oncogenes including Myc family genes and YAP1 and inactivation of tumor suppressor genes. We performed in-depth proteomic profiling of plasmas collected from 15 individuals with newly diagnosed early stage SCLC and from 15 individuals before the diagnosis of SCLC and compared findings with plasma proteomic profiles of 30 matched controls to determine the occurrence of signatures that reflect disease pathogenesis. A total of 272 proteins were elevated (area under the receiver operating characteristic curve (AUC) ≥ 0.60) among newly diagnosed cases compared to matched controls of which 31 proteins were also elevated (AUC ≥ 0.60) in case plasmas collected within one year prior to diagnosis. Ingenuity Pathway analyses of SCLC-associated proteins revealed enrichment of signatures of oncogenic MYC and YAP1. Intersection of proteins elevated in case plasmas with proteomic profiles of conditioned medium from 17 SCLC cell lines yielded 52 overlapping proteins characterized by YAP1-associated signatures of cytoskeletal re-arrangement and epithelial-to-mesenchymal transition. Among samples collected more than one year prior to diagnosis there was a predominance of inflammatory markers. Our integrated analyses identified novel circulating protein features in early stage SCLC associated with oncogenic drivers.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8391533PMC
http://dx.doi.org/10.3390/cancers13163972DOI Listing

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