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长期 DEHP/MEHP 暴露促进与糖基化改变相关的结直肠肿瘤干细胞特性。

Long-term DEHP/MEHP exposure promotes colorectal cancer stemness associated with glycosylation alterations.

机构信息

Institute of Basic Medical Science, College of Medicine, National Cheng Kung University, Tainan 70101, Taiwan; Department of Medical Laboratory Science and Biotechnology, College of Medicine, National Cheng Kung University, Tainan 70101, Taiwan.

Division of Colon and Rectal Surgery, Department of Surgery, E-DA Hospital, I-Shou University, Kaohsiung 82445, Taiwan; School of Medicine, College of Medicine, I-Shou University, Kaohsiung 82445, Taiwan.

出版信息

Environ Pollut. 2023 Jun 15;327:121476. doi: 10.1016/j.envpol.2023.121476. Epub 2023 Mar 28.

Abstract

Plasticizers are considered as environmental pollution released from medical devices and increased potential oncogenic risks in clinical therapy. Our previous studies have shown that long-term exposure to di-ethylhexyl phthalate (DEHP)/mono-ethylhexyl phthalate (MEHP) promotes chemotherapeutic drug resistance in colorectal cancer. In this study, we investigated the alteration of glycosylation in colorectal cancer following long-term plasticizers exposure. First, we determined the profiles of cell surface N-glycomes by using mass spectrometry and found out the alterations of α2,8-linkages glycans. Next, we analyzed the correlation between serum DEHP/MEHP levels and ST8SIA6 expression from matched tissues in total 110 colorectal cancer patients. Moreover, clinical specimens and TCGA database were used to analyze the expression of ST8SIA6 in advanced stage of cancer. Finally, we showed that ST8SIA6 regulated stemness in vitro and in vivo. Our results revealed long-term DEHP/MEHP exposure significantly caused cancer patients with poorer survival outcome and attenuated the expression of ST8SIA6 in cancer cells and tissue samples. As expected, silencing of ST8SIA6 promoted cancer stemness and tumorigenicity by upregulating stemness-associated proteins. In addition, the cell viability assay showed enhanced drug resistance in ST8SIA6 silencing cells treated with irinotecan. Besides, ST8SIA6 was downregulated in the advanced stage and positively correlated with tumor recurrence in colorectal cancer. Our results imply that ST8SIA6 potentially plays an important role in oncogenic effects with long-term phthalates exposure.

摘要

增塑剂被认为是医疗器械释放的环境污染物,并增加了临床治疗中的潜在致癌风险。我们之前的研究表明,长期接触邻苯二甲酸二乙酯(DEHP)/邻苯二甲酸单乙基己酯(MEHP)会促进结直肠癌细胞对化疗药物的耐药性。在这项研究中,我们研究了长期接触增塑剂后结直肠癌细胞糖基化的改变。首先,我们通过质谱法确定了细胞表面 N-糖组的图谱,发现了α2,8-连接聚糖的改变。接下来,我们分析了 110 例结直肠癌患者配对组织中血清 DEHP/MEHP 水平与 ST8SIA6 表达的相关性。此外,临床标本和 TCGA 数据库用于分析晚期癌症中 ST8SIA6 的表达。最后,我们表明 ST8SIA6 在体外和体内调节了肿瘤干细胞特性。我们的结果表明,长期 DEHP/MEHP 暴露显著导致癌症患者生存结局较差,并在癌细胞和组织样本中减弱了 ST8SIA6 的表达。正如预期的那样,沉默 ST8SIA6 通过上调与干细胞特性相关的蛋白质促进了肿瘤干细胞特性和肿瘤发生。此外,细胞活力测定显示,在沉默 ST8SIA6 的细胞中用伊立替康处理后,耐药性增强。此外,ST8SIA6 在结直肠癌的晚期下调,并与肿瘤复发呈正相关。我们的研究结果表明,ST8SIA6 在长期接触邻苯二甲酸酯引起的致癌作用中可能发挥重要作用。

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