Abstract | BACKGROUND: Gastric carcinoma is the most popular cancer worldwide. Anoctamin-1 is a calcium-activated channel and highly expressed in various tumors. A previous study indicated that suppressed Anoctamin-1 expression decreased cancer cell proliferation or migration. As a signal transduction and transcription activator, STAT6 is a novel agonist for Anoctamin-1 promoter. However, its role in tumor cell proliferation or migration remains unclear. Therefore, this study aimed to suppress STAT6 and Anoctamin-1 protein expression in gastric cancer cells to test the inhibitory effects on gastric cancer cell migration or invasion. MATERIALS AND METHODS: MTT colorimetry was used to test cell proliferation. Western blot was used to measure STAT6 and Anoctamin-1 expression before and after small interfering RNA ( siRNA) treatment. A scratch assay was performed to measure cell migration, followed by Transwell chamber assay analysis of cell invasion. RESULTS: CONCLUSIONS:
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Authors | Guohao Lu, Wanling Shi, Hongyu Zheng |
Journal | Cancer biotherapy & radiopharmaceuticals
(Cancer Biother Radiopharm)
Vol. 33
Issue 1
Pg. 3-7
(Feb 2018)
ISSN: 1557-8852 [Electronic] United States |
PMID | 29466035
(Publication Type: Journal Article)
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Chemical References |
- ANO1 protein, human
- Anoctamin-1
- Neoplasm Proteins
- RNA, Small Interfering
- STAT6 Transcription Factor
- STAT6 protein, human
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Topics |
- Anoctamin-1
(antagonists & inhibitors, biosynthesis, genetics)
- Cell Line, Tumor
- Cell Movement
(physiology)
- Cell Proliferation
(physiology)
- Gene Knockdown Techniques
- Humans
- Neoplasm Invasiveness
- Neoplasm Proteins
(antagonists & inhibitors, biosynthesis, genetics)
- RNA, Small Interfering
(administration & dosage, genetics)
- STAT6 Transcription Factor
(antagonists & inhibitors, biosynthesis, genetics)
- Stomach Neoplasms
(genetics, metabolism, pathology)
- Transfection
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