周期蛋白依赖激酶的基因特征:绝经前和绝经后妇女早期和晚期肺癌转移naïve的比较研究。

Q2 Biochemistry, Genetics and Molecular Biology Genes and Cancer Pub Date : 2021-02-10 eCollection Date: 2021-01-01 DOI:10.18632/genesandcancer.209
Muhammad Fazal Hussain Qureshi, Muzna Shah, Mahira Lakhani, Zain Jawed Abubaker, Danish Mohammad, Hira Farhan, Iman Zia, Rida Tafveez, Samahir Tariq Khan, Ghani Rubina, Mushtaq Shamim, Haider Ghulam
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引用次数: 1

摘要

人表皮生长因子受体2阳性(HER2+)乳腺癌(BC)是一种更具侵袭性的肿瘤,转移后的中位生存率为5年。尽管治疗成功,但不幸的是,大多数受影响的患者死亡。由细胞周期蛋白依赖性激酶(CDKs)控制的细胞周期和转录调节阶段的缺陷是许多癌症的标志,支持疾病的进展。因此,目前的研究观察了绝经前和绝经后肺转移BC组中六种CDKs mRNA表达水平的改变;多数为HER2+。选取200例绝经前和绝经后肺转移乳腺癌患者及健康对照者的血液进行RNA分离。定量PCR检测CDKs mRNA表达。我们观察到在绝经前和绝经后两组中CDK11、CDK12、CDK17、CDK18和CDK19过表达。然而,在两组患者中,CDK20从早期到晚期都表现出进行性下调。总的来说,这些数据揭示了CDKs过表达水平可能预测BC疾病进展,并为HER2+ BC癌症的新型抗癌策略提供了进一步的理论依据。
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Gene signatures of cyclin-dependent kinases: a comparative study in naïve early and advanced stages of lung metastasis breast cancer among pre- and post-menopausal women.

The Human epidermal growth factor receptor 2 positive (HER2+) breast cancer (BC) is a more aggressive tumor with 5 years median survival rates after metastasis. Despite successful treatment, unfortunately, the majority of affected patients die. Defects in cell cycle and transcription regulation phases which are governed by cyclin-dependent kinases (CDKs) are the hallmark of many cancers that underpinning the progression of the disease. Therefore, the current study looked at the alteration of six CDKs mRNA expression levels in pre- and postmenopausal lung metastasis BC groups; the majority were HER2+. Two hundred pre-and postmenopausal lung metastasis breast cancer and healthy control blood samples were taken for RNA isolation. Quantitative PCR was done for CDKs mRNA expressions. We observed overexpression of CDK11, CDK12, CDK17, CDK18, and CDK19 in both pre- and postmenopausal groups. However, CDK20 showed progressive downregulation from early to advanced stages in both groups of patients. Collectively, this data revealed that CDKs overexpression levels may predict BC disease progression and provide further rationale for novel anticancer strategies for HER2+ BC cancers.

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来源期刊
Genes and Cancer
Genes and Cancer Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.90
自引率
0.00%
发文量
6
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