| کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
|---|---|---|---|---|
| 2820519 | 1570081 | 2016 | 4 صفحه PDF | دانلود رایگان |
کلمات کلیدی
1.مقدمه
2. مواد و روش‌ها
2-1 جمعیت مطالعه
2-2 نمونه‌های بافت
2-3 استخراج RNA و روش RT-PCR کمّی
2-4 تحلیل آماری
جدول 1. ویژگی‌های بالینی بیماران (a: مرحله‌بندی تومور بر اساس طبقه‌بندی TNM انجام شد)
3. یافته‌ها
3-1 مشخصات بیمار
3-2 بیان ژن
4. بحث و بررسی
• It is important that we studied the biological role of the JAK/STAT signaling pathway in human colorectal tissue and we evaluated interactions with TNFα, NFκB, and caspase-3 in the research. We measured the mRNA levels of STAT1, TNF-α, TNF-α R1A, NFκB, and caspase-3 by RT-PCR. The STAT1, TNF-α, TNF-α R1A, and NFκB mRNA levels were increased in colorectal cancer tissue compared to adjacent normal colon tissue. These data support the importance of the JAK/STAT signaling pathway in colorectal cancer and suggest targets for intervention. We have new project to search other potentially related genes, pathways, and interactions. I hope we will send our new data to your journal in the future.
Colorectal cancer (CRC) constitutes a significant portion of mortality and morbidity due to cancer around the world. The present study was designed to evaluate the possible effects of the JAK/STAT, TNF-α, and NFκB pathways, and the caspase-3 apoptotic marker in human colorectal tissue. Data from tumor tissue and adjacent normal colon tissue (n:12) were obtained. Given the biological role of the JAK/STAT signaling pathway in human colorectal tissue, we evaluated interactions with TNFα, NFκB, and caspase-3. We measured the mRNA levels of STAT1, TNF-α, TNF-α R1A, NFκB, and caspase-3 by RT-PCR. The STAT1, TNF-α, TNF-α R1A, and NFκB mRNA levels were increased in colorectal cancer tissue compared to adjacent normal colon tissue (P < 0.01, P < 0.05, P < 0.05, and P < 0.05, respectively). There were no significant differences between colorectal cancer and adjacent normal colon tissue regarding the caspase-3 mRNA levels. STAT1 contributes to oncogenesis by promoting the progression of the cell cycle and preventing cells from undergoing apoptosis. In addition, TNF-α has proangiogenic activity and increases the neovascularization of tumors. According to our results, the mRNA levels of STAT1 and TNF-α were significantly higher in cancer tissues, but the mRNA levels of the apoptotic genes caspase-3 and 9 were similar to those of the normal colon tissue, suggesting that STAT1 and TNF-α are important components in the progression of colorectal cancer. These data support the importance of the JAK/STAT signaling pathway in colorectal cancer and suggest targets for intervention. We will be investigating potentially related genes, pathways, and interactions in our future studies.
Journal: Gene Reports - Volume 3, June 2016, Pages 1–4