4.7 Article

Telomere maintenance mechanism dysregulation serves as an early predictor of adjuvant therapy response and a potential therapeutic target in human cancers

Journal

INTERNATIONAL JOURNAL OF CANCER
Volume 151, Issue 2, Pages 313-327

Publisher

WILEY
DOI: 10.1002/ijc.34007

Keywords

adjuvant therapy; genomic instability; pan-cancer analysis; survival outcome; telomere maintenance mechanism

Categories

Funding

  1. Basic Scientific Research Funds of Heilongjiang Provincial Universities
  2. China Postdoctoral Science Foundation [2020M681111, 2021MD703831]
  3. Heilongjiang Postdoctoral Funds for Scientific Research [LBH-Z20168, LBH-Z20170]
  4. Heilongjiang Postdoctoral Young Talents Program [LBH-TZ2114]
  5. National Natural Science Foundation of China [62102122]
  6. Tou-Yan Innovation Team Program of the Heilongjiang Province [2019-15]

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Telomere maintenance mechanisms (TMMs) show consistent dysregulation across various cancers, and the TMScore based on TMM dysregulation is positively associated with tumor adverse features. Two prognostic patterns based on TMScore were identified for breast and lung cancer patients (poorer outcomes) and colon and stomach cancer patients (better outcomes). The prognostic value of TMScore remains significant regardless of whether patients received adjuvant therapy, and it can predict the effectiveness of adjuvant therapy.
Telomere maintenance mechanisms (TMMs) rescue cells from telomere crisis, endow cells immortal property, stabilize genomic integrity. However, TMM-associated molecular profiles and their clinical outcomes in cancer remain elusive. Here, we performed a pan-cancer and integrated analysis of TMM gene expression profiles from 10 107 unique samples with clinicopathological, molecular and outcome features across seven malignancies from the same microarray platform (Affymetrix GPL570 platform). This resource was divided into case-control datasets for obtaining dysregulated TMM genes and survival datasets for evaluating clinical outcomes. Multidimensional data from The Cancer Genome Atlas (TCGA) were used to elucidate associations between TMM dysregulation and survival, genomic instability. Our results demonstrated that TMMs had a consistent dysregulation spectrum across cancers, based on which we developed the TMM-dysregulation signature TMS score (TMScore) that was positively associated with various tumor adverse features. Two opposite prognostic patterns of TMScore independent of clinicopathological and molecular characteristics were identified, which might be explained by genomic instability: breast and lung cancer patients with elevated TMScore had inferior outcomes, suggesting TMScore-related genes as potential therapeutic targets, on the contrary, colon and stomach cancer patients had superior outcomes. Most important, the prognostic value of TMScore was still significant regardless of whether patients had received adjuvant therapy, which was valuable for discriminating nonresponders from responders, and could predict the effectiveness of adjuvant therapy. In summary, our resources delineate TMMs dysregulated landscape across cancers, shed light on the impact of TMMs dysregulation on patient outcomes and adjuvant therapy, and provide novel therapeutic opportunities for cancer treatment.

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