LncRNA MEG3 impacts proliferation, invasion, and migration of ovarian cancer cells through regulating PTEN
Objective and design We investigated the expressions of lncRNA MEG3 and PTEN in ovarian cancer tissues and their effects on cell proliferation, cycle and apoptosis of ovarian cancer. Methods Expression levels of MEG3 in ovarian cancer cell lines and normal ovarian cell lines were detected by qRT-PCR...
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Published in | Inflammation research Vol. 67; no. 11-12; pp. 927 - 936 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Cham
Springer International Publishing
01.12.2018
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | Objective and design
We investigated the expressions of lncRNA MEG3 and
PTEN
in ovarian cancer tissues and their effects on cell proliferation, cycle and apoptosis of ovarian cancer.
Methods
Expression levels of MEG3 in ovarian cancer cell lines and normal ovarian cell lines were detected by qRT-PCR. Cell viability was detected by MTT assay. Cell apoptosis and cell cycle distribution were measured by flow cytometry. Cell invasion capability was tested by transwell assay. Cell migration capacity was tested by wound healing. The xenograft model was constructed to explore the effect of lncRNA MEG3 on ovarian cancer in vivo.
Result
Compared with normal ovarian cells, expression levels of MEG3 and
PTEN
were relatively lower in ovarian cancer cells. There was a positive correlation between the expression of
PTEN
and the expression of MEG3. Enhanced expression level of
PTEN
suppressed SKOV3 cell proliferation, increased cell apoptosis rate, and decreased cell invasion and migration.
Conclusion
LncRNA MEG3 and
PTEN
were down-regulated in ovarian cancer cells. LncRNA MEG3 regulated the downstream gene
PTEN
in ovarian cancer cells to prohibit cell proliferation, promote apoptosis and block cell cycle progression. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 1023-3830 1420-908X 1420-908X |
DOI: | 10.1007/s00011-018-1186-z |