p53: A Key Protein That Regulates Pulmonary Fibrosis

Author:

Wu Qi1ORCID,Zhang Ke-jia23ORCID,Jiang Shi-min23ORCID,Fu Lu1ORCID,Shi Yue1ORCID,Tan Ru-bin1ORCID,Cui Jie1ORCID,Zhou Yao23ORCID

Affiliation:

1. Department of Physiology, Xuzhou Medical University, Xuzhou 221009, China

2. Department of Pathophysiology, Xuzhou Medical University, Xuzhou 221009, China

3. Laboratory of Clinical and Experimental Pathology, Xuzhou Medical University, Xuzhou 221009, China

Abstract

Pulmonary fibrosis is a progressively aggravating lethal disease that is a serious public health concern. Although the incidence of this disease is increasing, there is a lack of effective therapies. In recent years, the pathogenesis of pulmonary fibrosis has become a research hotspot. p53 is a tumor suppressor gene with crucial roles in cell cycle, apoptosis, tumorigenesis, and malignant transformation. Previous studies on p53 have predominantly focused on its role in neoplastic disease. Following in-depth investigation, several studies have linked it to pulmonary fibrosis. This review covers the association between p53 and pulmonary fibrosis, with the aim of providing novel ideas to improve the clinical diagnosis, treatment, and prognosis of pulmonary fibrosis.

Funder

Jiangsu Science and Technology Department

Publisher

Hindawi Limited

Subject

Cell Biology,Ageing,General Medicine,Biochemistry

Reference96 articles.

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