Plasma based protein signatures associated with small cell lung cancer

Johannes F. Fahrmann, Hiroyuki Katayama, Ehsan Irajizad, Ashish Chakraborty, Taketo Kato, Xiangying Mao, Soyoung Park, Eunice Murage, Leona Rusling, Chuan Yih Yu, Yinging Cai, Fu Chung Hsiao, Jennifer B. Dennison, Hai Tran, Edwin Ostrin, David O. Wilson, Jian Min Yuan, Jody Vykoukal, Samir Hanash

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

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 diag-nosis. 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 inflam-matory markers. Our integrated analyses identified novel circulating protein features in early stage SCLC associated with oncogenic drivers.

Original languageEnglish (US)
Article number3972
JournalCancers
Volume13
Issue number16
DOIs
StatePublished - Aug 2021

Keywords

  • Biomarkers
  • Proteomics
  • Small-cell lung cancer

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

MD Anderson CCSG core facilities

  • Biostatistics Resource Group

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