人类口腔癌中染色质修饰剂和组蛋白去乙酰化酶(HDAC’s)的芯片分析。

Chonnam Medical Journal Pub Date : 2021-09-01 Epub Date: 2021-09-24 DOI:10.4068/cmj.2021.57.3.176
Anand K Sajnani, Sanket G Shah, Mudasir Rashid, Abhiram Natu, Poonam B Gera, Sanjay Gupta
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引用次数: 4

摘要

组蛋白修饰已被证明在口腔鳞状细胞癌(OSCC)的表观遗传调控中发挥重要作用。对各种组蛋白乙酰转移酶(HATs)和组蛋白去乙酰化酶(HDACs)的癌症基因组图谱(TCGA)进行的计算机分析表明,HATs在正常和肿瘤样本之间没有差异,而HDAC2和HDAC1在正常和肿瘤样本之间分别有最大和最小的变化,HDAC6的表达没有变化。因此,本研究旨在验证HDAC 1、2和6 mrna在印度队列口腔黏膜和舌头SCC样本中的表达状态。对组织病理学完整的口腔黏膜和舌鳞癌组织进行RNA分离和cDNA合成,并进行q-PCR检测hdac。舌组织样品的平均RNA产率为~ 2µg/mg, A260/280比值在2.03 ~ 2.06之间。口腔黏膜组织样本的平均RNA产率为~ 1µg/mg, A260/280比值在2.00 ~ 2.08之间。我们已经证明HDAC2在舌和颊粘膜样本中过表达。HDAC2的过表达暗示了在口腔癌治疗中HDACi与标准化疗药物的潜在应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

<i>In-Silico</i> Analysis of Chromatin Modifiers and Profiling of Histone Deacetylases (HDAC's) in Human Oral Cancer.

<i>In-Silico</i> Analysis of Chromatin Modifiers and Profiling of Histone Deacetylases (HDAC's) in Human Oral Cancer.

<i>In-Silico</i> Analysis of Chromatin Modifiers and Profiling of Histone Deacetylases (HDAC's) in Human Oral Cancer.

In-Silico Analysis of Chromatin Modifiers and Profiling of Histone Deacetylases (HDAC's) in Human Oral Cancer.

Histone modifications have been demonstrated to play a significant role in oral squamous cell carcinoma (OSCC) epigenetic regulation. An in-silico analysis of The Cancer Genome Atlas (TCGA) of various histone acetyl transferases (HATs) and histone deacetylases (HDACs) suggested that HATs do not differ between normal and tumor samples whereas HDAC2 and HDAC1 change maximally and marginally respectively between normal and tumor patients with no change being noted in HDAC6 expression. Hence, this investigation was carried out to validate the expression states of HDAC 1, 2 and 6 mRNAs in buccal mucosa and tongue SCC samples in an Indian cohort. Buccal mucosa and tongue squamous cell carcinoma tissues with intact histopathology were processed for RNA isolation followed by cDNA synthesis which was then subjected to q-PCR for HDACs. The average RNA yield of the tongue tissue sample was ∼2 µg/mg of tissue and the A260/280 ratios were between 2.03 and 2.06. The average RNA yield of buccal mucosa tissue sample was ∼1 µg/mg of tissue and the A260/280 ratio were between 2.00 and 2.08. We have demonstrated that HDAC2 was overexpressed in tongue and buccal mucosa samples. Over-expression of HDAC2 imply potential use of HDACi along with standard chemotherapeutic drug in oral cancer treatment.

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