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Circulating adipose stromal cells as a response biomarker in phase II energy balance trials of obese breast cancer survivors and high-risk women. | LitMetric

AI Article Synopsis

  • Scientists studied special cells called CASC that are found in the blood and may help tumors grow, especially in people who are overweight.
  • They looked at 33 women at risk for breast cancer and found that more CASC cells were in women with higher body weight.
  • In breast cancer survivors who lost weight, they noticed that as they lost belly fat, the number of these cells also decreased, which could help in future health studies.

Article Abstract

Purpose: Circulating adipose stromal cells (CASC) are thought to be increased in obesity and facilitate angiogenesis, and tumor metastases.

Methods: CASC were identified from buffy coat peripheral blood mononuclear cells (PBMCs) by flow cytometry as CD34CD31 CD45 and CASC frequency was compared to adiposity measures in 33 women at increased risk for breast cancer. Feasibility of CASC as a response biomarker for a diet and exercise intervention in ten breast cancer survivors was then explored.

Results: For 33 high-risk women, median CASC frequency was 9.7 per million PBMCs and trended positively with body mass index, fat mass index (FMI), and percent android fat. Correlation was significant when BMI was dichotomized at > versus < 35 kg/m (p = 0.02). For ten breast cancer survivors with a median BMI of 37 kg/m, median CASC frequency was 16.4 per million PBMCs. In univariate analyses, change in BMI, total fat and visceral fat were significantly correlated with change in CASC frequency. On multivariate analysis, change in visceral adipose had the strongest association with change in CASC frequency (p < 0.00078).

Conclusions: The association between the reduction in visceral adipose tissue and the decrease in frequency of circulating adipose stromal cells suggests that the latter might be a useful biomarker in clinical trials of obese breast cancer survivors undergoing a weight loss intervention.

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Source
http://dx.doi.org/10.1007/s10549-019-05251-7DOI Listing

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