Purpose To investigate the effect of silencing the YKL-40 gene on the expression of inflammatory factors and the effect of silencing the YKL-40 gene of THP-1 cells on endometrial cancer. Methods We used a siRNA targeting a sequence in YKL-40 (si-YKL-40) to transfect HEC-1A and THP-1 cells. Quantitative real-time polymerase chain reaction assay was performed to investigate the mRNA levels of YKL-40, IL-8 and MMP-9 in HEC-1A and THP-1 cells. Migration, and invasion assays were performed to identify the effects of co-culture with THP-1 cells that silenced YKL-40 gene on the migration and invasion capacity of HEC-1A cells. Tube formation ability were detected by Matrigel-based angiogenesis assay. Results We successfully transfected HEC-1A and THP-1 cells with lentivirus to silence the YKL-40 gene. Compared with the blank control group and NC group, the expression of YKL-40, IL-8 and MMP-9 which were examined by qRT-PCR in YKL-40-siRNA group was significantly reduced in the two cell lines; after co-cultured with the supernatant of transfected THP-1 cells, the migration and invasion ability of HEC-1A cells in YKL-40-siRNA group was significantly reduced; the number of tubes in the YKL-40-siRNA group was significantly reduced, the spacing between the tubes was significantly increased, and the structure of tubes was incomplete. Conclusion Silencing the YKL-40 gene in THP-1 cells can inhibit the expression of inflammatory factors, the invasion and migration of human endometrial cancer cells and the capacity of vitro angiogenic. And YKL-40 gene as a marker of inflammation may be an effective therapeutic target for endometrial cancer.
机构:
Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Ctr Immunobiol, Boston, MA 02215 USAHarvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Ctr Immunobiol, Boston, MA 02215 USA
Grey, ST
Csizmadia, V
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Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Ctr Immunobiol, Boston, MA 02215 USAHarvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Ctr Immunobiol, Boston, MA 02215 USA
Csizmadia, V
Hancock, WW
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Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Ctr Immunobiol, Boston, MA 02215 USAHarvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Ctr Immunobiol, Boston, MA 02215 USA
机构:
Sichuan Univ, W China Hosp Stomatol, State Key Lab Oral Dis, Chengdu, Sichuan, Peoples R ChinaSichuan Univ, W China Hosp Stomatol, State Key Lab Oral Dis, Chengdu, Sichuan, Peoples R China
Li, Lei
Drury, Jeanie L.
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Univ Washington, Dept Restorat Dent, Sch Dent, Seattle, WA 98195 USASichuan Univ, W China Hosp Stomatol, State Key Lab Oral Dis, Chengdu, Sichuan, Peoples R China
Drury, Jeanie L.
Zhang, Hai
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Univ Washington, Dept Restorat Dent, Sch Dent, Seattle, WA 98195 USASichuan Univ, W China Hosp Stomatol, State Key Lab Oral Dis, Chengdu, Sichuan, Peoples R China
Zhang, Hai
Sun, Jianxun
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Sichuan Univ, W China Hosp Stomatol, State Key Lab Oral Dis, Chengdu, Sichuan, Peoples R ChinaSichuan Univ, W China Hosp Stomatol, State Key Lab Oral Dis, Chengdu, Sichuan, Peoples R China
Sun, Jianxun
DiJulio, Dennis
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Univ Washington, Dept Oral Hlth Sci, Sch Dent, Seattle, WA 98195 USASichuan Univ, W China Hosp Stomatol, State Key Lab Oral Dis, Chengdu, Sichuan, Peoples R China
DiJulio, Dennis
Chung, Whasun O.
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Univ Washington, Dept Oral Hlth Sci, Sch Dent, Seattle, WA 98195 USASichuan Univ, W China Hosp Stomatol, State Key Lab Oral Dis, Chengdu, Sichuan, Peoples R China
Chung, Whasun O.
Wataha, John C.
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Univ Washington, Dept Restorat Dent, Sch Dent, Seattle, WA 98195 USASichuan Univ, W China Hosp Stomatol, State Key Lab Oral Dis, Chengdu, Sichuan, Peoples R China