scholarly journals Effects of metformin on cell proliferation and apoptosis in human esophageal squamous cancer cell line Eca109

2013 ◽  
Vol 21 (36) ◽  
pp. 4075
Author(s):  
Feng Liang ◽  
Chang-Cheng Wang ◽  
Su-Juan Fei
Tumor Biology ◽  
2011 ◽  
Vol 32 (4) ◽  
pp. 801-808 ◽  
Author(s):  
Wei Guo ◽  
Ying-Bo Zou ◽  
Yao-Guang Jiang ◽  
Ru-Wen Wang ◽  
Yun-Ping Zhao ◽  
...  

Author(s):  
Hai-Bo Zhou ◽  
Wang-Qian Ma ◽  
Li-Ming Shao

Objective: To investigate the effect of t (11; 19) (q23; p13.1) gene on proliferation and apoptosis 0f SGC 7901 gastric cancer cell line Methods: Gastric cancer cell line SGC 7901 cells were selected to transfect t (11; 19) (q23; p13.1) gene. MRNA levels of t (11; 19) (q23; p13.1) in each group were regulated after 24, 48 and 72h byRT- PCR. Cell proliferation was determined MTT assay. The apoptosis status of the SGC 7901 cells was detected TUNEL method. Immunohistochemical staining evaluated the expression of apoptotic genes Bcl-2 and Bax. Results: The MTT assay showed that t (11; 19) (q23; p13.1) decreased the proliferation of SGC 7901 cells. TUNEL method detected t (11; 19) (q23; p13.1) could improve apoptosis of SGC 7901 cells. In addition, t (11; 19) (q23; p13.1) could improve the expression of apoptotic gene Bcl-2 and reduce the expression of apoptotic gene Bax. Conclusion: T (11; 19) (q23; p13.1) gene can inhibit gastric cancer cell proliferation and improve apoptosis of gastric cancer cell.


2012 ◽  
Vol 12 (8) ◽  
pp. 950-961 ◽  
Author(s):  
Yang Qiu ◽  
Ying-Bo Zou ◽  
Kun Li ◽  
Yao-Guang Jiang ◽  
Kang Yang ◽  
...  

2001 ◽  
Vol 280 (5) ◽  
pp. C1083-C1089 ◽  
Author(s):  
Yingjie Yu ◽  
Arun K. Rishi ◽  
Jerrold R. Turner ◽  
Dayou Liu ◽  
Eric D. Black ◽  
...  

Although epidermal growth factor receptor (EGFR) plays a key role in regulating cell proliferation, differentiation, and transformation in many tissues, little is known about the factor(s) that may modulate its function. We have isolated a cDNA clone from the rat gastroduodenal mucosa whose full length revealed 1,958 bp that contained 227 bp of 5′-untranslated region (UTR) and an open-reading frame encoding 479 amino acids, followed by 290 bp of 3′-UTR. It showed ∼85% nucleotide homology to the external domain of the rat EGFR. We refer to the product of the newly isolated cDNA as EGFR-related protein (ERRP). In Northern blot analysis with poly(A)+ RNA from different rat tissues, ERRP cDNA hybridized to several mRNA transcripts with the strongest reaction noted with a transcript of ∼2 kb. Maximal expression of the 2-kb mRNA transcript was observed in the small intestine, followed by colon, liver, gastric mucosa, and other tissues. Transfection of ERRP cDNA into a colon cancer cell line, HCT116, resulted in a marked reduction in proliferation in monolayer and colony formation in soft agar compared with the vector-transfected controls. In another colon cancer cell line, Caco-2, with a tetracycline-regulated promoter system, induction of ERRP expression in the absence of doxycycline was associated with a marked reduction in EGFR activation and proliferation. We conclude that the ERRP cDNA may represent a new member of the EGFR gene family and that ERRP plays a role in regulating cell proliferation by modulating the function of EGFR.


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