Spasmolytic polypeptide‐expressing metaplasia (SPEM) cell lineages can be an origin of gastric cancer

Author:

Goldenring James R1234ORCID

Affiliation:

1. Section of Surgical Sciences Vanderbilt University Medical Center Nashville TN USA

2. Epithelial Biology Center Vanderbilt University Medical Center Nashville TN USA

3. Department of Cell and Developmental Biology Vanderbilt University School of Medicine Nashville TN USA

4. Nashville VA Medical Center Nashville TN USA

Abstract

AbstractIntestinal‐type gastric cancer arises in a field of precancerous metaplastic lineages. Two types of metaplastic glands are found in the stomachs of humans with the characteristics of pyloric metaplasia or intestinal metaplasia. While spasmolytic polypeptide‐expressing metaplasia (SPEM) cell lineages have been identified in both pyloric metaplasia and incomplete intestinal metaplasia, it has been unclear whether SPEM lineages or intestinal lineages can give rise to dysplasia and cancer. A recent article published in The Journal of Pathology describes a patient with evidence of an activating Kras(G12D) mutation in SPEM that is propagated into adenomatous and cancerous lesions which manifest further oncogenic mutations. This case therefore supports the concept that SPEM lineages can serve as a direct precursor for dysplasia and intestinal‐type gastric cancer. © 2023 The Pathological Society of Great Britain and Ireland.

Funder

National Cancer Institute

National Institute of Diabetes and Digestive and Kidney Diseases

U.S. Department of Defense

U.S. Department of Veterans Affairs

Publisher

Wiley

Subject

Pathology and Forensic Medicine

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