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血清剪接因子脯氨酸和谷氨酸丰富是诊断非小细胞肺癌和其他实体瘤的标志物。

Serum Splicing Factor Proline- and Glutamine-Rich Is a Diagnostic Marker for Non-Small-Cell Lung Cancer and Other Solid Cancers.

机构信息

Department of Medicine, University of Minnesota, Minneapolis, MN 55455, USA.

Hematology, Oncology and Transplantation, School of Medicine, University of Minnesota, 420 Delaware Street, SE, Minneapolis, MN 55455, USA.

出版信息

Int J Mol Sci. 2024 Aug 12;25(16):8766. doi: 10.3390/ijms25168766.

Abstract

Cancer markers are measurable molecules in blood or tissues that are produced by tumor cells or immune cells in response to cancer progression. They play an important role in clinical diagnosis, prognosis, and therapy monitoring. Splicing factor proline- and glutamine-rich (SFPQ) plays an important role in cancer growth and metastasis. SFPQ is not only more highly expressed in non-small-cell lung cancer (NSCLC) cells than it is in controls, but also highly expressed in cancer cells in patients with other solid cancers. Thus, a new enzyme-linked immunosorbent assay (ELISA) for detecting SFPQ was developed, in which the SFPQ protein is trapped by the first specific mAb coated on a microplate, and then recognized by a second specific mAb. This assay allows for the specific detection of SFPQ in the serum of patients with solid cancer. Regarding NSCLC, the serum SFPQ levels distinguished the non-cancer controls from the patients with NSCLC, with an area under the curve of 0.876, a sensitivity of 87%, and a specificity of 94%. The serum SFPQ levels were significantly elevated in the patients with NSCLC or other solid cancers. In conclusion, serum SFPQ could be a promising novel diagnostic biomarker for NSCLC and other malignancies.

摘要

肿瘤标志物是血液或组织中可测量的分子,由肿瘤细胞或免疫细胞产生,以响应癌症的进展。它们在临床诊断、预后和治疗监测中发挥着重要作用。拼接因子脯氨酸和谷氨酰胺丰富(SFPQ)在癌症生长和转移中起着重要作用。SFPQ 不仅在非小细胞肺癌(NSCLC)细胞中的表达水平高于对照,而且在其他实体癌患者的癌细胞中也高度表达。因此,开发了一种新的酶联免疫吸附测定(ELISA)来检测 SFPQ,其中 SFPQ 蛋白被涂覆在微孔板上的第一个特异性 mAb 捕获,然后被第二个特异性 mAb 识别。该测定法允许在患有实体癌的患者的血清中特异性地检测 SFPQ。关于 NSCLC,血清 SFPQ 水平将非癌症对照与 NSCLC 患者区分开来,曲线下面积为 0.876,灵敏度为 87%,特异性为 94%。患有 NSCLC 或其他实体癌的患者的血清 SFPQ 水平显著升高。总之,血清 SFPQ 可能是 NSCLC 和其他恶性肿瘤有前途的新型诊断生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/668f/11354699/62026559c888/ijms-25-08766-g001.jpg

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