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Crosstalk between pancreatic cancer and adipose tissue: Molecular mechanisms and therapeutic implications.

Biochemical and biophysical research communications 2024 Vol.740() p. 151012

Diao B, Fan Z, Zhou B, Zhan H

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The incidence rate of pancreatic cancer, a fatal illness with a meager 5-year survival rate, has been on the rise in recent times.

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APA Diao B, Fan Z, et al. (2024). Crosstalk between pancreatic cancer and adipose tissue: Molecular mechanisms and therapeutic implications.. Biochemical and biophysical research communications, 740, 151012. https://doi.org/10.1016/j.bbrc.2024.151012
MLA Diao B, et al.. "Crosstalk between pancreatic cancer and adipose tissue: Molecular mechanisms and therapeutic implications.." Biochemical and biophysical research communications, vol. 740, 2024, pp. 151012.
PMID 39561650

Abstract

The incidence rate of pancreatic cancer, a fatal illness with a meager 5-year survival rate, has been on the rise in recent times. When individuals accumulate excessive amounts of adipose tissue, the adipose organ becomes dysfunctional due to alterations in the adipose tissue microenvironment associated with inflammation and metabolism. This phenomenon may potentially contribute to the aberrant accumulation of fat that initiates pancreatic carcinogenesis, thereby influencing the disease's progression, resistance to treatment, and metastasis. This review presents a summary of the impact of pancreatic steatosis, visceral fat, cancer-associated adipocytes and lipid diets on the advancement of pancreatic cancer, as well as the reciprocal effects of pancreatic cancer on adipose tissue. Understanding the molecular mechanisms underlying the relationship between dysfunctional adipose tissue and pancreatic cancer better may lead to the discovery of new therapeutic targets for the disease's prevention and individualized treatment. This is especially important given the rising global incidence of obesity, which will improve the pancreatic cancer treatment options that are currently insufficient.

MeSH Terms

Humans; Pancreatic Neoplasms; Adipose Tissue; Animals; Obesity; Tumor Microenvironment; Adipocytes

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