Senescence-associated secretory phenotype determines survival and therapeutic response in cervical cancer

Sharad Purohit, Wenbo Zhi, Daron G. Ferris, Manual Alverez, Lynn Kim Hoang Tran, Paul Minh Huy Tran, Boying Dun, Diane Hopkins, Bruno Dos Santos, Sharad Ghamande, Jin-Xiong She

Research output: Contribution to journalArticlepeer-review

14 Scopus citations

Abstract

Molecular biomarkers that can predict survival and therapeutic outcome are still lacking for cervical cancer. Here we measured a panel of 19 serum proteins in sera from 565 patients with stage II or III cervical cancer and identified 10 proteins that have an impact on disease specific survival (DSS) (Hazzard’s ratio; HR = 1.51–2.1). Surprisingly, all ten proteins are implicated in senescence-associated secreted phenotype (SASP), a hallmark of cellular senescence. Machine learning using Ridge regression of these SASP proteins can robustly stratify patients with high SASP, which is associated with poor survival, and patients with low SASP associated with good survival (HR = 3.09–4.52). Furthermore, brachytherapy, an effective therapy for cervical cancer, greatly improves survival in SASP-high patients (HR = 3.3, p < 5 × 10−5) but has little impact on survival of SASP-low patients (HR = 1.5, p = 0.31). These results demonstrate that cellular senescence is a major determining factor for survival and therapeutic response in cervical cancer and suggest that senescence reduction therapy may be an efficacious strategy to improve the therapeutic outcome of cervical cancer.

Original languageEnglish (US)
Article number2899
Pages (from-to)1-19
Number of pages19
JournalCancers
Volume12
Issue number10
DOIs
StatePublished - Oct 2020

Keywords

  • Biomarkers
  • Cervical neoplasia
  • Gynecologic cancers
  • Prognosis
  • Proteomics
  • Radiation therapy
  • Serum proteins

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

Fingerprint

Dive into the research topics of 'Senescence-associated secretory phenotype determines survival and therapeutic response in cervical cancer'. Together they form a unique fingerprint.

Cite this