Literature DB >> 29172956

Estrogen and insulin synergistically promote type 1 endometrial cancer progression.

Wenyan Tian1, Fei Teng1, Jing Zhao1, Jinping Gao1, Chao Gao1, Dandan Sun1, Guoyan Liu1, Yanfang Zhang1, Shizhu Yu2, Wei Zhang3, Yingmei Wang1, Fengxia Xue1.   

Abstract

Despite evidence that estrogens and insulin are related to type 1 endometrial carcinoma (EC), their synergistic role has not been analyzed. Here, we investigated how estrogens cooperate with insulin to promote type 1 EC progression. We examined the clinical significance of serum estrogen and insulin levels using type 1 EC patients and control subjects. Univariate and multivariate logistic regression analyses for total, premenopausal, and postmenopausal subjects were performed. Type 1 EC risk was evaluated with respect to estrone, estradiol, and insulin levels based on odds ratios (ORs) using stratified data. Cell growth in vitro and in vivo, effects of insulin and estradiol on apoptosis and cell cycle distribution were measured after estradiol and insulin stimulation. Estrone and insulin concentrations were significantly high in type 1 EC patients and retained positive associations with type 1 EC after adjustment for BMI, WHR, diabetes, and hypertension. The odds ratio was significantly high for type 1 EC patients with higher levels of estrone/estradiol and insulin than for patients with higher levels of either estrone/estradiol or insulin, suggesting that estrogen and insulin play a synergistic role in type 1 EC carcinogenesis and progression. Compared to EC cells and cell-based xenografts treated with estradiol or insulin alone, those treated with estradiol and insulin exhibited stronger stimulation. Estrogen and insulin play synergistic roles in type 1 EC carcinogenesis and progression, extending our understanding of EC risks.

Entities:  

Keywords:  cell lines; estrogen; insulin; synergistic risk; type 1 endometrial cancer (EC)

Mesh:

Substances:

Year:  2017        PMID: 29172956      PMCID: PMC5718804          DOI: 10.1080/15384047.2017.1394547

Source DB:  PubMed          Journal:  Cancer Biol Ther        ISSN: 1538-4047            Impact factor:   4.742


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