scholarly journals A tRNA-derived fragment from Chinese yew suppresses ovarian cancer growth via targeting TRPA1

Author(s):  
Kai-Yue Cao ◽  
Tong-Meng Yan ◽  
Ji-Zhou Zhang ◽  
Ting-Fung Chan ◽  
Jie Li ◽  
...  
Keyword(s):  
2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Mei Song ◽  
Oladapo O. Yeku ◽  
Sarwish Rafiq ◽  
Terence Purdon ◽  
Xue Dong ◽  
...  

AbstractImmunosuppressive tumor microenvironment (TME) and ascites-derived spheroids in ovarian cancer (OC) facilitate tumor growth and progression, and also pose major obstacles for cancer therapy. The molecular pathways involved in the OC-TME interactions, how the crosstalk impinges on OC aggression and chemoresistance are not well-characterized. Here, we demonstrate that tumor-derived UBR5, an E3 ligase overexpressed in human OC associated with poor prognosis, is essential for OC progression principally by promoting tumor-associated macrophage recruitment and activation via key chemokines and cytokines. UBR5 is also required to sustain cell-intrinsic β-catenin-mediated signaling to promote cellular adhesion/colonization and organoid formation by controlling the p53 protein level. OC-specific targeting of UBR5 strongly augments the survival benefit of conventional chemotherapy and immunotherapies. This work provides mechanistic insights into the novel oncogene-like functions of UBR5 in regulating the OC-TME crosstalk and suggests that UBR5 is a potential therapeutic target in OC treatment for modulating the TME and cancer stemness.


Neoplasia ◽  
2018 ◽  
Vol 20 (12) ◽  
pp. 1209-1218 ◽  
Author(s):  
Kari E Hacker ◽  
Danielle E Bolland ◽  
Lijun Tan ◽  
Anjan K Saha ◽  
Yashar S Niknafs ◽  
...  

2010 ◽  
Vol 70 (21) ◽  
pp. 8927-8936 ◽  
Author(s):  
Monique A. Spillman ◽  
Nicole G. Manning ◽  
Wendy W. Dye ◽  
Carol A. Sartorius ◽  
Miriam D. Post ◽  
...  

Oncogene ◽  
2018 ◽  
Vol 37 (35) ◽  
pp. 4854-4870 ◽  
Author(s):  
Rashid Gabbasov ◽  
Fang Xiao ◽  
Caitlin G. Howe ◽  
Laura E. Bickel ◽  
Shane W. O’Brien ◽  
...  

JCI Insight ◽  
2017 ◽  
Vol 2 (18) ◽  
Author(s):  
Mingzhu Yin ◽  
Huanjiao Jenny Zhou ◽  
Jiqin Zhang ◽  
Caixia Lin ◽  
Hongmei Li ◽  
...  

2017 ◽  
Vol 13 (6) ◽  
pp. 4039-4046 ◽  
Author(s):  
Ping Liu ◽  
Xiaorong Qi ◽  
Ce Bian ◽  
Fan Yang ◽  
Xiaojuan Lin ◽  
...  
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2015 ◽  
Vol 13 (1) ◽  
Author(s):  
Xiuli Li ◽  
Fang Gu ◽  
Chenguang Niu ◽  
Yuanfen Wang ◽  
Zhongyu Liu ◽  
...  

2012 ◽  
Vol 22 (3) ◽  
pp. 386-393 ◽  
Author(s):  
Fei Liang ◽  
Qingtao Lü ◽  
Shuyu Sun ◽  
Jie Zhou ◽  
Vladimir M. Popov ◽  
...  

ObjectiveThis study aimed to determine the functional relationship between the levels of dachshund homolog 1 (DACH1) expression and different subtypes of ovarian cancer and to investigate the possible prognostic value of DACH1 in ovarian cancer.MethodsImmunohistochemical staining was deployed to determine the protein levels of DACH1. Staining was performed on patient samples, for whom the detailed follow-up data have been acquired during the last 10 years. Normal, benign, borderline, cancer, and metastatic ovarian cancer samples were included in this study.ResultsThe results of our study show that DACH1 protein levels increase with the invasiveness of the ovarian cancer. As the cancer progresses from benign and borderline to metastatic, DACH1 protein expression increases as well. Moreover, with the increase in expression, the subcellular distribution of DACH1 changes from nucleus in normal tissue to cytoplasm in cancer. Finally, DACH1 expression levels were compared with estrogen receptor α (ERα) levels, and the results showed that overall DACH1 levels were higher, whereas also DACH1 exhibited increased cytoplasmic expression in ERα-positive ovarian cancer samples.ConclusionsThese results indicate that DACH1 is highly expressed in metastatic ovarian cancer compared with that of normal, benign, and borderline ovarian tissues and that it could play an important role in cancer growth.


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