结直肠癌患者化疗及血浆脂肪因子水平。

IF 0.3
Grzegorz Słomian, Elżbieta Świętochowska, Grzegorz Nowak, Krystyna Pawlas, Aleksandra Żelazko, Przemysław Nowak
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引用次数: 17

摘要

脂肪因子是由脂肪组织产生和分泌的分子,与多种恶性肿瘤有关。脂肪因子可以抑制或促进不同类型癌症的特定细胞行为。本研究的目的是探讨化疗对结直肠癌(CRC)患者选择脂肪因子的影响。收集了42例病理证实的晚期结直肠癌患者的血液样本,这些患者需要姑息性化疗。化疗前和化疗后3个月,采用ELISA法测定各组瘦素、脂联素、抵抗素和脂肪素水平。在评估的42例患者中,18例达到部分缓解(PR), 16例达到疾病稳定(SD), 8例出现疾病进展(PD)。我们发现,以5-氟尿嘧啶为基础的化疗方案显著增加了PR和SD患者血浆中瘦素和脂联素的水平,降低了血浆中抵抗素和内脏素的水平,而PD患者血浆中这些分子的水平没有受到影响。此外,PD患者化疗前后的平均血浆瘦素水平明显低于PR和SD患者,抵抗素和visfatin的平均血浆水平明显高于PR和SD患者。我们得出结论,姑息性化疗在结直肠癌患者中,除了提供临床益处外,还积极影响PR和SD患者的细胞因子产生和分泌。具体来说,我们发现姑息性化疗增加了抗炎脂肪因子脂联素的血浆水平,降低了血浆中visfatin和抵抗素的水平,这两种分子在PR和SD患者中促进血管生成和癌细胞增殖。此外,瘦素、视脂素和抵抗素的基线值可能作为化疗不良反应的预后指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chemotherapy and plasma adipokines level in patients with colorectal cancer.

Adipokines are molecules produced and secreted by adipose tissue and are linked to multiple malignancies. Adipokines can suppress or promote particular cell behaviors in different types of cancer. The aim of this study was to investigate the impact of chemotherapy on select adipokines in patients with colorectal cancer (CRC). Blood samples were collected from 42 patients with pathologically documented advanced CRC, who required palliative chemotherapy. Leptin, adiponectin, resistin and visfatin levels were measured by ELISA before and 3 months after the administration of chemotherapy. Among the 42 patients evaluated, 18 achieved a partial response (PR), 16 achieved stable disease (SD) and 8 patients experienced disease progression (PD). We found that 5-fluorouracil-based chemotherapy regimens significantly increased plasma levels of leptin and adiponectin and decreased plasma levels of resistin and visfatin in PR and SD patients, whereas the plasma levels of these molecules were not affected in PD patients. Furthermore, the mean plasma levels of leptin were significantly lower, and the mean plasma levels of resistin and visfatin were significantly greater in patients with PD compared with PR and SD both before and after chemotherapy treatment. We conclude that palliative chemotherapy in CRC patients, in addition to providing clinical benefits, positively affects cytokine production and secretion in PR and SD patients. Specifically, we found that palliative chemotherapy increased plasma levels of the anti-inflammatory adipokine adiponectin and decreased the plasma levels of visfatin and resistin, molecules known to promote angiogenesis and cancer cell proliferation in PR and SD patients. Moreover, the baseline values of leptin, visfatin and resistin might serve as prognostic indicators of a poor response to chemotherapy.

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