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MARCKSL1 作为淋巴结阴性乳腺癌患者预后因素的验证研究。

Validation study of MARCKSL1 as a prognostic factor in lymph node-negative breast cancer patients.

机构信息

Department of Pathology, Stavanger University Hospital, Stavanger, Norway.

Department of Chemistry, Bioscience and Environmental Engineering, University of Stavanger, Stavanger, Norway.

出版信息

PLoS One. 2019 Mar 11;14(3):e0212527. doi: 10.1371/journal.pone.0212527. eCollection 2019.

Abstract

Protein expression of Myristoylated alanine-rich C kinase substrate like-1 (MARCKSL1) has been identified as a prognostic factor in lymph-node negative (LN-) breast cancer patients. We aim to validate MARCKSL1 protein expression as a prognostic marker for distant metastasis-free survival (DMFS) in a new cohort of LN- breast cancer patients. MARCKSL1 expression was evaluated in 151 operable T1,2N0M0 LN- breast cancer patients by immunohistochemistry. Median follow-up time was 152 months, range 11-189 months. Results were compared with classical prognosticators (age, tumor diameter, grade, estrogen receptor, and proliferation) using single (Kaplan-Meier) and multivariate (Cox model) survival analysis. Thirteen patients (9%) developed distant metastases. With both single and multiple analysis of all features, MARCKSL1 did not show a significant prognostic value for DMFS (p = 0.498). Of the assessed classical prognosticators, only tumor diameter showed prognostic value (hazard ratio 9.3, 95% confidence interval 2.8-31.0, p <0.001). MARCKSL1 expression could not be confirmed as a prognostic factor in this cohort. Possible reasons include changes in diagnostic and treatment guidelines between the discovery and validation cohorts. Further studies are needed to reveal the potential biological role of this protein in breast cancer.

摘要

Myristoylated alanine-rich C kinase substrate like-1 (MARCKSL1) 的蛋白表达已被确定为淋巴结阴性(LN-)乳腺癌患者的预后因素。我们旨在通过免疫组织化学方法验证 MARCKSL1 蛋白表达在新的 LN-乳腺癌患者中作为无远处转移生存(DMFS)的预后标志物。评估了 151 例可手术的 T1、2N0M0 LN-乳腺癌患者的 MARCKSL1 表达。中位随访时间为 152 个月,范围为 11-189 个月。结果与经典预后因素(年龄、肿瘤直径、分级、雌激素受体和增殖)进行了单因素(Kaplan-Meier)和多因素(Cox 模型)生存分析。13 例(9%)患者发生远处转移。通过单一和多种因素分析所有特征,MARCKSL1 对 DMFS 无显著预后价值(p = 0.498)。在评估的经典预后因素中,只有肿瘤直径具有预后价值(风险比 9.3,95%置信区间 2.8-31.0,p <0.001)。在本队列中,MARCKSL1 表达不能被确认为预后因素。可能的原因包括发现和验证队列之间诊断和治疗指南的变化。需要进一步的研究来揭示该蛋白在乳腺癌中的潜在生物学作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9448/6411117/0ab6cdcf2626/pone.0212527.g001.jpg

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