4.6 Review

Isoforms of the p53 Family and Gastric Cancer: A Menage a Trois for an Unfinished Affair

Journal

CANCERS
Volume 13, Issue 4, Pages -

Publisher

MDPI
DOI: 10.3390/cancers13040916

Keywords

p53 family; isoforms; gastric cancer; biomarker; personalized therapy; chemotherapy; immunotherapy; metastasis; cell death; tumor ecosystem

Categories

Funding

  1. Inserm
  2. CNRS
  3. Ligue Contre le Cancer
  4. Itmo Cancer
  5. Idex Unistra
  6. Alsace Contre le Cancer
  7. IdEx Unistra [ANR-10-IDEX-0002]
  8. SFRI-STRAT'US project [ANR-20-SFRI-0012]

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The p53 family plays a crucial role in gastric cancer, but its complexity results in uncertainty in treatment efficacy and the lack of predictive markers, leading to predominantly cytotoxic chemotherapy and low response rates to immunotherapy for a minority of patients.
Simple Summary The p53 family is a complex family of transcription factors with different cellular functions that are involved in several physiological processes. A massive amount of data has been accumulated on their critical role in the tumorigenesis and the aggressiveness of cancers of different origins. If common features are observed, there are numerous specificities that may reflect particularities of the tissues from which the cancers originated. In this regard, gastric cancer tumorigenesis is rather remarkable, as it is induced by bacterial and viral infections, various chemical carcinogens, and familial genetic alterations, which provide an example of the variety of molecular mechanisms responsible for cell transformation and how they impact the p53 family. This review summarizes the knowledge gathered from over 40 years of research on the role of the p53 family in gastric cancer, which still displays one of the most elevated mortality rates amongst all types of cancers. Gastric cancer is one of the most aggressive cancers, with a median survival of 12 months. This illustrates its complexity and the lack of therapeutic options, such as personalized therapy, because predictive markers do not exist. Thus, gastric cancer remains mostly treated with cytotoxic chemotherapies. In addition, less than 20% of patients respond to immunotherapy. TP53 mutations are particularly frequent in gastric cancer (+/- 50% and up to 70% in metastatic) and are considered an early event in the tumorigenic process. Alterations in the expression of other members of the p53 family, i.e., p63 and p73, have also been described. In this context, the role of the members of the p53 family and their isoforms have been investigated over the years, resulting in conflicting data. For instance, whether mutations of TP53 or the dysregulation of its homologs may represent biomarkers for aggressivity or response to therapy still remains a matter of debate. This uncertainty illustrates the lack of information on the molecular pathways involving the p53 family in gastric cancer. In this review, we summarize and discuss the most relevant molecular and clinical data on the role of the p53 family in gastric cancer and enumerate potential therapeutic innovative strategies.

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