Re‐expression of Lactotransferrin, a candidate tumor suppressor inactivated by promoter hypermethylation, impairs the malignance of oral squamous cell carcinoma cells. (5th November 2014)
- Record Type:
- Journal Article
- Title:
- Re‐expression of Lactotransferrin, a candidate tumor suppressor inactivated by promoter hypermethylation, impairs the malignance of oral squamous cell carcinoma cells. (5th November 2014)
- Main Title:
- Re‐expression of Lactotransferrin, a candidate tumor suppressor inactivated by promoter hypermethylation, impairs the malignance of oral squamous cell carcinoma cells.
- Authors:
- Zhang, Jie
Ling, Tianyou
Wu, Hanjiang
Wang, Kai - Abstract:
- <abstract abstract-type="main" id="jop12279-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="jop12279-sec-0001" sec-type="section"> <title>Background</title> <p> <italic>Lactotransferrin</italic> (<italic>LTF</italic>) has been confirmed to act as a tumor suppressor in multiple cancers; however, its roles in oral squamous cell carcinoma (OSCC), one of malignant head and neck carcinomas, has not been explored.</p> </sec> <sec id="jop12279-sec-0002" sec-type="section"> <title>Methods</title> <p>Here, the expression of <italic>LTF</italic> in OSCC tissues and TCA8113 cells was detected with RT‐PCR, qPCR, and IHC. And the correlation between LTF expression and OSCC metastasis was assessed. MS‐PCR was performed to reveal the methylation status in promoter regions of <italic>LTF</italic> both in OSCC tissue samples and cells. The influences of 5‐Aza‐Cdc treatment to the methylation status and expression levels of <italic>LTF</italic> were also analyzed. At last, the functions of <italic>LTF</italic> in OSCC progression were demonstrated by MTT analysis, clone formation assay, and cell cycle analysis in TCA8113 cells with forced ectopic expression of <italic>LTF</italic>.</p> </sec> <sec id="jop12279-sec-0003" sec-type="section"> <title>Results</title> <p> <italic>LTF</italic> showed a low or null expression pattern in OSCC tissues and cells, at least partially, due to the hypermethylated status in promoter regions for 5‐Aza‐Cdc, a methyltransferase<abstract abstract-type="main" id="jop12279-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="jop12279-sec-0001" sec-type="section"> <title>Background</title> <p> <italic>Lactotransferrin</italic> (<italic>LTF</italic>) has been confirmed to act as a tumor suppressor in multiple cancers; however, its roles in oral squamous cell carcinoma (OSCC), one of malignant head and neck carcinomas, has not been explored.</p> </sec> <sec id="jop12279-sec-0002" sec-type="section"> <title>Methods</title> <p>Here, the expression of <italic>LTF</italic> in OSCC tissues and TCA8113 cells was detected with RT‐PCR, qPCR, and IHC. And the correlation between LTF expression and OSCC metastasis was assessed. MS‐PCR was performed to reveal the methylation status in promoter regions of <italic>LTF</italic> both in OSCC tissue samples and cells. The influences of 5‐Aza‐Cdc treatment to the methylation status and expression levels of <italic>LTF</italic> were also analyzed. At last, the functions of <italic>LTF</italic> in OSCC progression were demonstrated by MTT analysis, clone formation assay, and cell cycle analysis in TCA8113 cells with forced ectopic expression of <italic>LTF</italic>.</p> </sec> <sec id="jop12279-sec-0003" sec-type="section"> <title>Results</title> <p> <italic>LTF</italic> showed a low or null expression pattern in OSCC tissues and cells, at least partially, due to the hypermethylated status in promoter regions for 5‐Aza‐Cdc, a methyltransferase inhibitor, could restore the expression of <italic>LTF</italic> in TCA8113 cells. And the expression level of <italic>LTF</italic> exhibited a negative correlation with OSCC metastasis.</p> </sec> <sec id="jop12279-sec-0004" sec-type="section"> <title>Conclusions</title> <p>Re‐expression of <italic>LTF</italic> inhibited the growth, proliferation, as well as cell cycle progression of TCA8113 cells. In conclusion, hypermethylation contributes much to <italic>LTF</italic> inactivation in OSCC. And <italic>LTF</italic> can partially reverse the malignant phenotypes of OSCC cells and may be served as a potential target for diagnosis and therapy of OSCC in future.</p> </sec> </abstract> … (more)
- Is Part Of:
- Journal of oral pathology & medicine. Volume 44:Number 8(2015:Sep.)
- Journal:
- Journal of oral pathology & medicine
- Issue:
- Volume 44:Number 8(2015:Sep.)
- Issue Display:
- Volume 44, Issue 8 (2015)
- Year:
- 2015
- Volume:
- 44
- Issue:
- 8
- Issue Sort Value:
- 2015-0044-0008-0000
- Page Start:
- 578
- Page End:
- 584
- Publication Date:
- 2014-11-05
- Subjects:
- Dentistry -- Periodicals
Teeth -- Diseases -- Periodicals
617 - Journal URLs:
- http://www.blackwell-synergy.com/rd.asp?goto=journal&code=jop ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/jop.12279 ↗
- Languages:
- English
- ISSNs:
- 0904-2512
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5026.435000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4356.xml