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November 6, 2023EMBO ReportsOpen Access

Breast adipose tissue‐derived extracellular vesicles from obese women alter tumor cell metabolism

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Why the study?

Breast adipose tissue is an important contributor to the obesity-breast cancer link, but the role of adipose-derived extracellular vesicles in modulating tumor cell function is not fully understood.

Population

Breast cancer cells and extracellular vesicles from breast adipose tissue of overweight or obese women

Comparison

EVs from overweight or obese women vs EVs from lean women

Design

Preclinical in vitro study

Key result

Extracellular vesicles from breast adipose tissue of overweight or obese women increased breast cancer cell proliferation and mitochondrial respiration via the Akt/mTOR/P70S6K pathway.

Authors

SLShuchen LiuABAlberto Benito‐MartínFVFanny A. Pelissier Vatter

Discussion

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Member takes

Overview

O-EVs promote breast cancer cell proliferation in vitro; hypothesis-generating for EV roles in obesity-breast cancer progression.

Structured PICO

P
Population
Breast cancer cells exposed to extracellular vesicles (EVs) obtained from breast adipose tissue of women who are overweight or obese (O-EVs) or lean women.
E
Exposure
Exposure to O-EVs (extracellular vesicles from overweight/obese women's breast adipose tissue); metformin treatment.
C
Comparator
Exposure to EVs from lean women.
O
Outcome
Tumor cell proliferation and metabolic reprogramming (mitochondrial respiration, gene expression).surrogate

Extracellular vesicles from breast adipose tissue of obese women promote breast cancer cell proliferation and mitochondrial respiration via the Akt/mTOR/P70S6K pathway.

Cite This Study

Liu et al. (2023) studied Breast cancer and obesity. Extracellular vesicles from breast adipose tissue of overweight or obese women (O-EVs) vs. Extracellular vesicles from lean women was evaluated on Tumor cell proliferation and mitochondrial respiration. Extracellular vesicles from breast adipose tissue of overweight or obese women increased breast cancer cell proliferation and mitochondrial respiration via the Akt/mTOR/P70S6K pathway.

synapsesocial.com/papers/6a947a598d39fd7482c7d78bhttps://doi.org/10.15252/embr.202357339
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