Srinivasan Srimeenakshi, Godin Biana
Department of Nanomedicine, Houston Methodist Research Institute, Houston, TX 77030, USA.
Department of Obstetrics and Gynecology, Houston Methodist Hospital, Houston, TX 77030, USA.
Cancers (Basel). 2019 Jul 9;11(7):961. doi: 10.3390/cancers11070961.
Over-expression of Crk-like protein (CrkL), an intracellular adaptor protein, in breast cancer biopsies has been linked to poor prognosis. CrkL can be secreted from cancer cells binding to β1 integrin on the cell membrane. In this study, we evaluated, for the first time, the levels of soluble CrkL in serum of breast cancer patients. Expression of CrkL and secreted fractions from human breast cancer cell lines and clinical patient samples were assessed by immunohistochemistry and Enzyme Linked Immuno-Sorbent Assay (ELISA). CrkL levels in tissues and sera of patients with different disease stages were compared and statistically analyzed by Chi-square test and Student's -test. Culture media from human breast cancer cell lines SUM159, MDA-MB231, and MCF7 showed over a 21-, 15-, and 11-fold higher concentration of soluble CrkL as compared to normal breast epithelium cell line MCF10A. Expression of CrkL was elevated in 85% of breast tumor tissue sections. Serum levels of CrkL were significantly higher in breast cancer patients than in healthy donors. All patients with metastatic disease had significantly elevated concentration of soluble CrkL in the serum with on average three-fold increase from the baseline. The data suggest that soluble fraction of CrkL can be further evaluated as a serum biomarker for advanced disease in breast cancer patients.
细胞内衔接蛋白类Crk蛋白(CrkL)在乳腺癌活检组织中的过表达与预后不良有关。CrkL可从癌细胞分泌出来,与细胞膜上的β1整合素结合。在本研究中,我们首次评估了乳腺癌患者血清中可溶性CrkL的水平。通过免疫组织化学和酶联免疫吸附测定(ELISA)评估了人乳腺癌细胞系和临床患者样本中CrkL的表达及分泌组分。采用卡方检验和学生t检验对不同疾病阶段患者组织和血清中的CrkL水平进行比较和统计分析。与正常乳腺上皮细胞系MCF10A相比,人乳腺癌细胞系SUM159、MDA-MB231和MCF7的培养基中可溶性CrkL浓度分别高出21倍、15倍和11倍以上。85%的乳腺肿瘤组织切片中CrkL表达升高。乳腺癌患者血清中的CrkL水平显著高于健康供体。所有转移性疾病患者血清中可溶性CrkL浓度均显著升高,平均比基线水平增加了三倍。数据表明,CrkL的可溶性组分可作为乳腺癌患者晚期疾病的血清生物标志物进行进一步评估。