Nam Sang Eun, Ko Young-Sin, Park Kyoung Sik, Jin TongYi, Yoo Young-Bum, Yang Jung-Hyun, Kim Wook-Youn, Han Hye-Seung, Lim So-Dug, Lee Seung Eun, Kim Wan-Seop
Department of Surgery, Konkuk University School of Medicine, Seoul, Korea.
Research Institute of Medical Science, Konkuk University School of Medicine, Seoul, Korea.
Ann Surg Treat Res. 2022 Aug;103(2):63-71. doi: 10.4174/astr.2022.103.2.63. Epub 2022 Aug 5.
Triple-negative breast cancer (TNBC) is an aggressive subtype of breast cancer with a poor prognosis and a lack of targeted therapy. Overexpression of is thought to be associated with this aggressive subtype of cancer. Here, we performed a comprehensive analysis and assessed the association between overexpression of and TNBC.
First, using different web-based bioinformatics platforms (TIMER 2.0, UALCAN, and GEPIA 2), the expression of was assessed. Then, the expression of the protein and hormone receptors and HER2 status were assessed by immunohistochemical analysis. For samples of tumors with equivocal immunoreactivity, we performed silver hybridization of the HER2 gene to determine an accurate HER2 status. Next, we used the R package and bc-GenExMiner 4.8 to analyze the relationship between expression and clinicopathological parameters in breast cancer patients. Finally, we determined the relationship between overexpression and prognosis in patients.
The expression of in breast cancer tissues is significantly higher than in normal tissue. expression was significantly related to worse overall survival (P < 0.05) and was correlated with these clinicopathological features: T stage, N stage, age, high histologic grade, estrogen receptor status, progesterone receptor status, Her-2 status, TNBC status, basal-like status, CK5/6 status, and Ki67 status.
was overexpressed in breast cancer compared to normal tissue, and it may be involved in the progression of breast cancer malignancy. This study provides suggestive evidence of the prognostic role of in breast cancer and the therapeutic target for TNBC.
三阴性乳腺癌(TNBC)是一种侵袭性乳腺癌亚型,预后较差且缺乏靶向治疗。[具体基因名称]的过表达被认为与这种侵袭性癌症亚型相关。在此,我们进行了全面分析并评估了[具体基因名称]过表达与TNBC之间的关联。
首先,使用不同的基于网络的生物信息学平台(TIMER 2.0、UALCAN和GEPIA 2)评估[具体基因名称]的表达。然后,通过免疫组织化学分析评估[具体基因名称]蛋白、激素受体和HER2状态的表达。对于免疫反应性不明确的肿瘤样本,我们进行HER2基因的银[具体技术名称]杂交以确定准确的HER2状态。接下来,我们使用R包和bc - GenExMiner 4.8分析[具体基因名称]表达与乳腺癌患者临床病理参数之间的关系。最后,我们确定了[具体基因名称]过表达与患者预后之间的关系。
乳腺癌组织中[具体基因名称]的表达明显高于正常组织。[具体基因名称]表达与较差的总生存期显著相关(P < 0.05),并与这些临床病理特征相关:T分期、N分期、年龄、高组织学分级、雌激素受体状态、孕激素受体状态、Her - 2状态、TNBC状态、基底样状态、CK5/6状态和Ki67状态。
与正常组织相比,[具体基因名称]在乳腺癌中过表达,并且它可能参与乳腺癌恶性进展。本研究为[具体基因名称]在乳腺癌中的预后作用和TNBC的治疗靶点提供了提示性证据。