Low Expression of Stanniocalcin 1 (STC-1) Protein Is Associated With Poor Clinicopathologic Features of Endometrial Cancer.

Pathology oncology research : POR Pub Date : 2021-09-28 eCollection Date: 2021-01-01 DOI:10.3389/pore.2021.1609936
Masuma Khatun, Elina Urpilainen, Anne Ahtikoski, Riikka K Arffman, Annukka Pasanen, Ulla Puistola, Juha S Tapanainen, Leif C Andersson, Ralf Butzow, Mikko Loukovaara, Terhi T Piltonen
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引用次数: 4

Abstract

Stanniocalcin-1 (STC-1) is a glycoprotein hormone involved in diverse biological processes, including regulation of calcium phosphate homeostasis, cell proliferation, apoptosis, inflammation, oxidative stress responses, and cancer development. The role of STC-1 in endometrial cancer (EC) is yet to be elucidated. In this study, we investigated the protein expression pattern of STC-1 in a tissue microarray (TMA) cohort of hysterectomy specimens from 832 patients with EC. We then evaluated the prognostic value of STC-1 expression regarding the clinicopathologic features and patients survival over a period of 140 months. Our results revealed that in EC tissue samples, STC-1 is mainly localized in the endometrial epithelium, although some expression was also observed in the stroma. Decreased STC-1 expression was associated with factors relating to a worse prognosis, such as grade 3 endometrioid tumors (p = 0.030), deep myometrial invasion (p = 0.003), lymphovascular space invasion (p = 0.050), and large tumor size (p = 0.001). Moreover, STC-1 expression was decreased in tumors obtained from obese women (p = 0.014) and in women with diabetes mellitus type 2 (DMT2; p = 0.001). Interestingly, the data also showed an association between DNA mismatch repair (MMR) deficiency and weak STC-1 expression, specifically in the endometrial epithelium (p = 0.048). No association was observed between STC-1 expression and disease-specific survival. As STC-1 expression was particularly low in cases with obesity and DMT2 in the TMA cohort, we also evaluated the correlation between metformin use and STC-1 expression in an additional EC cohort that only included women with DMT2 (n = 111). The analysis showed no difference in STC-1 expression in either the epithelium or the stroma in women undergoing metformin therapy compared to metformin non-users. Overall, our data may suggest a favorable role for STC-1 in EC behavior; however, further studies are required to elucidate the detailed mechanism and possible applications to cancer treatment.

Abstract Image

Abstract Image

STC-1蛋白低表达与子宫内膜癌不良临床病理特征相关
STC-1是一种糖蛋白激素,参与多种生物过程,包括调控磷酸钙稳态、细胞增殖、凋亡、炎症、氧化应激反应和癌症发展。STC-1在子宫内膜癌(EC)中的作用尚未阐明。在这项研究中,我们通过组织微阵列(TMA)研究了832例EC患者子宫切除术标本中STC-1的蛋白表达模式。在140个月的时间里,我们评估了STC-1表达在临床病理特征和患者生存方面的预后价值。我们的研究结果显示,在EC组织样本中,STC-1主要定位于子宫内膜上皮,尽管在间质中也观察到一些表达。STC-1表达降低与预后较差的因素相关,如3级子宫内膜样肿瘤(p = 0.030)、深部肌层浸润(p = 0.003)、淋巴血管间隙浸润(p = 0.050)和肿瘤大(p = 0.001)。此外,STC-1在肥胖女性和2型糖尿病女性(DMT2;P = 0.001)。有趣的是,数据还显示DNA错配修复(MMR)缺陷与STC-1弱表达之间存在关联,特别是在子宫内膜上皮中(p = 0.048)。未观察到STC-1表达与疾病特异性生存之间的关联。由于TMA队列中肥胖和DMT2患者的STC-1表达特别低,我们还在另一个仅包括DMT2患者的EC队列中评估了二甲双胍使用与STC-1表达之间的相关性(n = 111)。分析显示,接受二甲双胍治疗的女性与未使用二甲双胍的女性相比,上皮或间质中STC-1的表达没有差异。总的来说,我们的数据可能表明STC-1在EC行为中起着有利的作用;然而,需要进一步的研究来阐明其详细的机制和可能在癌症治疗中的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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