scholarly journals G9a Is SETting the Stage for Colorectal Oncogenesis

Genes ◽  
2020 ◽  
Vol 11 (6) ◽  
pp. 616
Author(s):  
Christopher J. Bergin ◽  
Yannick D. Benoit

Recently, Kato et al. reported recurrent activating mutations in the SET domain of histone methyltransferase G9a, driving an oncogenic cascade in melanoma. The authors also reported correlations between G9a expression and the regulation of the canonical WNT pathway. Although we could not observe such mutations in human colorectal adenocarcinoma, newly reported findings are of high relevance to colorectal cancer, as WNT target gene signatures were closely associated with G9a expression. Here, we put into perspective such new results on G9a expression in colorectal cancers and the potential relationship with tumor heterogeneity and acquisition of neoplastic stemness.

2015 ◽  
Vol 148 (4) ◽  
pp. S-572 ◽  
Author(s):  
Zhenzhen Wen ◽  
Song Xu ◽  
Shujiong Feng ◽  
Haiying Tao ◽  
Tianhui Pan ◽  
...  

2013 ◽  
Vol 108 (8) ◽  
pp. 1750-1756 ◽  
Author(s):  
G Piazzi ◽  
M Selgrad ◽  
M Garcia ◽  
C Ceccarelli ◽  
L Fini ◽  
...  

Cancers ◽  
2021 ◽  
Vol 13 (14) ◽  
pp. 3437
Author(s):  
Hee Eun Kang ◽  
Yoojeong Seo ◽  
Jun Seop Yun ◽  
Sang Hyun Song ◽  
Dawool Han ◽  
...  

The Wnt and Hippo pathways are tightly coordinated and understanding their reciprocal regulation may provide a novel therapeutic strategy for cancer. Anti-helminthic niclosamide is an effective inhibitor of Wnt and is now in a phase II trial for advanced colorectal cancer (CRC) patients. We found that Axin2, an authentic target gene of canonical Wnt, acts as aYAP phosphorylation activator in APC-mutated CRC. While niclosamide effectively suppresses Wnt, it also inhibits Hippo, limiting its therapeutic potential for CRC. To overcome this limitation, we utilized metformin, a clinically available AMPK activator. This combinatory approach not only suppresses canonical Wnt activity, but also inhibits YAP activity in CRC cancer cells and in patient-derived cancer organoid through the suppression of cancer stemness. Further, combinatory oral administration suppressed in vivo tumorigenesis and the cancer progression of APC-MIN mice models. Our observations provide not only a reciprocal link between Wnt and Hippo, but also clinically available novel therapeutics that are able to target Wnt and YAP in APC-mutated CRC.


2005 ◽  
Vol 65 (14) ◽  
pp. 6199-6206 ◽  
Author(s):  
Aykut Üren ◽  
Shannon Fallen ◽  
Hang Yuan ◽  
Alp Usubütün ◽  
Türkan Küçükali ◽  
...  

2009 ◽  
Vol 28 (2) ◽  
pp. 121-122
Author(s):  
D. Takashi ◽  
B. John ◽  
P. Prem ◽  
T. Jennifer

Biochimie ◽  
2014 ◽  
Vol 106 ◽  
pp. 149-156 ◽  
Author(s):  
Cheng-gui Miao ◽  
Ying-ying Yang ◽  
Xu He ◽  
Cheng Huang ◽  
Yan Huang ◽  
...  

2010 ◽  
pp. OR38-3-OR38-3
Author(s):  
Carles Gaston-Massuet ◽  
Cynthia L Andoniadou ◽  
Massimo Signore ◽  
Sajutha Jayakody ◽  
Nicoletta Charolidi ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document