4.5 Article

TP53 signature diagnostic system using multiplex reverse transcription-polymerase chain reaction system enables prediction of prognosis of breast cancer patients

Journal

BREAST CANCER
Volume 28, Issue 6, Pages 1225-1234

Publisher

SPRINGER JAPAN KK
DOI: 10.1007/s12282-021-01250-z

Keywords

TP53 signature; Breast cancer; Prognostic factor; Diagnostic system

Funding

  1. JSPS KAKENHI [24701000]
  2. Research funds for preventive medicine from Miyagi Health Care Association
  3. Grants-in-Aid for Scientific Research [24701000] Funding Source: KAKEN

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The study developed a simple diagnostic system for determining TP53 signature status. Patients with TP53 mutant signature had significantly shorter recurrence-free survival compared to those with TP53 wild-type signature, and the signature was found to be an independent predictor of recurrence-free survival in breast cancer patients.
Background TP53 status based on TP53 signature, a gene expression profile to determine the presence or absence of TP53 mutation, is an independent prognostic factor of breast cancer. The purpose of this study was to develop a simple diagnostic system for TP53 signature status. Methods We developed a multiplex reverse transcription-polymerase chain reaction system to determine TP53 status. Based on this system, prospectively collected 189 patients with stage I and II breast cancer were determined to have TP53 mutant signature or TP53 wild-type signature. The prognostic significance of the TP53 signature by the diagnostic system was analyzed. Results The diagnostic accuracy of TP53 status and reproducibility of this diagnosis system was confirmed. Using the diagnostic system, 89 patients were classified as TP53 mutant signature and the remaining 100 cases were classified as TP53 wild-type signature. Recurrence-free survival (RFS) among patients with TP53 mutant signature was significantly shorter than that among those with TP53 wild-type signature. On univariate and multivariate analyses, the TP53 signature status was an independent predictor of RFS. RFS among patients with TP53 mutant signature was significantly shorter than that among those with TP53 wild-type signature in a cohort of estrogen receptor-positive breast cancer. Although a difference was not significant, no recurrent cases was observed in TP53 wild-type signature group in triple negative breast cancer. Conclusion This simple and precise diagnostic system to determine TP53 signature status may help in prognostic assessment, therapeutic decision-making, and treatment optimization in patients with breast cancer.

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