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Cited by in CrossRef
For: Wanitsuwan W, Kanngurn S, Boonpipattanapong T, Sangthong R, Sangkhathat S. Overall expression of beta-catenin outperforms its nuclear accumulation in predicting outcomes of colorectal cancers. World J Gastroenterol 2008; 14(39): 6052-6059 [PMID: 18932285 DOI: 10.3748/wjg.14.6052]
URL: https://www.wjgnet.com/1007-9327/full/v14/i39/6052.htm
Number Citing Articles
1
Ehsan Nazemalhosseini Mojarad, Seyed Mohammad Hossein Kashfi, Hanieh Mirtalebi, Shohre Almasi, Vahid Chaleshi, Roya Kishani Farahani, Peyman Tarban, Mahsa Molaei, Mohammad Reza Zali, Peter J.K. Kuppen. Prognostic Significance of Nuclear β-Catenin Expression in Patients with Colorectal Cancer from Iran. Iranian Red Crescent Medical Journal 2015; 17(7) doi: 10.5812/ircmj.22324v2
2
Yifan Tai, Emma L. Woods, Jordanna Dally, Deling Kong, Robert Steadman, Ryan Moseley, Adam C. Midgley. Myofibroblasts: Function, Formation, and Scope of Molecular Therapies for Skin Fibrosis. Biomolecules 2021; 11(8) doi: 10.3390/biom11081095
3
Xu Wang, Ke Chen, Zhenglin Wang, Yuanmin Xu, Longfei Dai, Tao Bai, Bo Chen, Wenqi Yang, Wei Chen. Using Immune-Related Long Non-coding Ribonucleic Acids to Develop a Novel Prognosis Signature and Predict the Immune Landscape of Colon Cancer. Frontiers in Cell and Developmental Biology 2021; 9 doi: 10.3389/fcell.2021.750709
4
Weitao Zhang, Lu Kong, Hongbin Zhu, Decong Sun, Quanli Han, Bin Yan, Zhi Cui, Weiwei Zhang, Shurong Zhang, Xindan Kang, Guanghai Dai, Niansong Qian, Wenji Yan. Retinoic Acid-Induced 2 (RAI2) Is a Novel Antagonist of Wnt/β-Catenin Signaling Pathway and Potential Biomarker of Chemosensitivity in Colorectal Cancer. Frontiers in Oncology 2022; 12 doi: 10.3389/fonc.2022.805290
5
Jarle Bruun, Matthias Kolberg, Jahn M. Nesland, Aud Svindland, Arild Nesbakken, Ragnhild A. Lothe. Prognostic Significance of β-Catenin, E-Cadherin, and SOX9 in Colorectal Cancer: Results from a Large Population-Representative Series. Frontiers in Oncology 2014; 4 doi: 10.3389/fonc.2014.00118
6
Laura Saieva, Maria Magdalena Barreca, Chiara Zichittella, Maria Giulia Prado, Marco Tripodi, Riccardo Alessandro, Alice Conigliaro. Hypoxia-Induced miR-675-5p Supports β-Catenin Nuclear Localization by Regulating GSK3-β  Activity in Colorectal Cancer Cell Lines. International Journal of Molecular Sciences 2020; 21(11) doi: 10.3390/ijms21113832
7
Xiao-yan Zhang, Lin Wang, Yuhuan Qiao, Ruixia Guo. Expressions of sFRP1 and β-Catenin in Cervical Cancer. Journal of Medical Biochemistry 2012; 31(1) doi: 10.2478/v10011-011-0040-4
8
Linna Wang, Dan Li, Yang Liu, Yuan Wang, Jinfeng Cui, Airong Cui, Wenxin Wu. Expression of RUNX3 and β-catenin in the carcinogenesis of sporadic colorectal tubular adenoma. Tumor Biology 2014; 35(6) doi: 10.1007/s13277-014-1800-9
9
Bryan D. White, Andy J. Chien, David W. Dawson. Dysregulation of Wnt/β-Catenin Signaling in Gastrointestinal Cancers. Gastroenterology 2012; 142(2) doi: 10.1053/j.gastro.2011.12.001
10
Ling Wang, Ke Deng, Liang Gong, Liang Zhou, Sapna Sayed, Huan Li, Qi Sun, Zijie Su, Zhongyuan Wang, Shanshan Liu, Huifang Zhu, Jiaxing Song, Desheng Lu. Chlorquinaldol targets the β-catenin and T-cell factor 4 complex and exerts anti-colorectal cancer activity. Pharmacological Research 2020; 159 doi: 10.1016/j.phrs.2020.104955
11
Larissa Belov, Jerry Zhou, Richard I. Christopherson. Cell Surface Markers in Colorectal Cancer Prognosis. International Journal of Molecular Sciences 2010; 12(1) doi: 10.3390/ijms12010078
12
Jian-Hong Peng, Yu-Jing Fang, Cai-Xia Li, Qing-Jian Ou, Wu Jiang, Shi-Xun Lu, Zhen-Hai Lu, Pei-Xing Li, Jing-Ping Yun, Rong-Xin Zhang, Zhi-Zhong Pan, De-Sen Wan. A scoring system based on artificial neural network for predicting 10-year survival in stage II A colon cancer patients after radical surgery. Oncotarget 2016; 7(16) doi: 10.18632/oncotarget.8217
13
Eunjoo Kim, Laurie A Davidson, Roger S Zoh, Martha E Hensel, Michael L Salinas, Bhimanagouda S Patil, Guddadarangavvanahally K Jayaprakasha, Evelyn S Callaway, Clinton D Allred, Nancy D Turner, Brad R Weeks, Robert S Chapkin. Rapidly cycling Lgr5+ stem cells are exquisitely sensitive to extrinsic dietary factors that modulate colon cancer risk. Cell Death & Disease 2016; 7(11) doi: 10.1038/cddis.2016.269
14
Tianqi Gao, Mengping Li, Dailin Wu, Ni Xiao, Dan Huang, Li Deng, Lunwei Yang, Chunhong Tian, Yang Cao, Jun Zhang, Jihong Gu, Yang Yu. Exploring the pathogenesis of colorectal carcinoma complicated with hepatocellular carcinoma via microarray data analysis. Frontiers in Pharmacology 2023; 14 doi: 10.3389/fphar.2023.1201401
15
Sakarias Wangefjord, Jenny Brändstedt, Kajsa Ericson Lindquist, Björn Nodin, Karin Jirström, Jakob Eberhard. Associations of beta-catenin alterations and MSI screening status with expression of key cell cycle regulating proteins and survival from colorectal cancer. Diagnostic Pathology 2013; 8(1) doi: 10.1186/1746-1596-8-10
16
Neeladrisingha Das, Neelanjana Ray, Abhinandan R. Patil, Shashank Sagar Saini, Bhairavnath Waghmode, Chandrachur Ghosh, Sunita B. Patil, Sandeep B. Patil, Chandrasekhar S. Mote, Surendra Saini, B. L. Saraswat, Debabrata Sircar, Partha Roy. Inhibitory effect of selected Indian honey on colon cancer cell growth by inducing apoptosis and targeting the β-catenin/Wnt pathway. Food & Function 2022; 13(15) doi: 10.1039/D1FO03727G
17
Wenhao Weng, Junlan Feng, Huanlong Qin, Yanlei Ma. Molecular therapy of colorectal cancer: Progress and future directions. International Journal of Cancer 2015; 136(3) doi: 10.1002/ijc.28722
18
E. M. Paltseva, A. V. Varlamov, M. I. Sekacheva, D. N. Fedorov, O. G. Skipenko. Impact of preoperative drug therapy on adhesion molecule expression in colorectal cancer liver metastases. Arkhiv patologii 2015; 77(3) doi: 10.17116/patol201577310-16
19
Argjira Juniku-Shkololli. A Critical Evaluation of Vitamin D - Clinical Overview. 2017;  doi: 10.5772/67397
20
Shangxin Zhang, Deguan Li, Min Zhao, Fei Yang, Changye Sang, Changhong Yan, Zhenjun Wang, Yongxiang Li. Exosomal miR-183-5p Shuttled by M2 Polarized Tumor-Associated Macrophage Promotes the Development of Colon Cancer via Targeting THEM4 Mediated PI3K/AKT and NF-κB Pathways. Frontiers in Oncology 2021; 11 doi: 10.3389/fonc.2021.672684
21
Xiaoying Zheng, Jianhua Ren, Bingjun Peng, Junling Ye, Xinchun Wu, Wenhui Zhao, Yanjun Li, Ruihui Chen, Xue Gong, Chengmei Bai, Yating Wang, Haiyun Zhao, Yiqing Zhang. MALAT1 overexpression promotes the growth of colon cancer by repressing β-catenin degradation. Cellular Signalling 2020; 73 doi: 10.1016/j.cellsig.2020.109676
22
Liang Duan, Rui Wu, Liwei Ye, Haiyan Wang, Xia Yang, Yunyuan Zhang, Xian Chen, Guowei Zuo, Yan Zhang, Yaguang Weng, Jinyong Luo, Min Tang, Qiong Shi, Tongchuan He, Lan Zhou, Jun Sun. S100A8 and S100A9 Are Associated with Colorectal Carcinoma Progression and Contribute to Colorectal Carcinoma Cell Survival and Migration via Wnt/β-Catenin Pathway. PLoS ONE 2013; 8(4) doi: 10.1371/journal.pone.0062092
23
Motomichi Fujita, Hideo Suzuki, Fumio Fukai. Involvement of integrin-activating peptides derived from tenascin-C in colon cancer progression. World Journal of Gastrointestinal Oncology 2021; 13(9): 980-994 doi: 10.4251/wjgo.v13.i9.980
24
Jing-Xia Chang, Meng Zhang, Li-Li Lou, He-Ying Chu, Hua-Qi Wang. KIS, a target of SOX4, regulates the ID1-mediated enhancement of β-catenin to facilitate lung adenocarcinoma cell proliferation and metastasis. Journal of Cancer Research and Clinical Oncology 2024; 150(7) doi: 10.1007/s00432-024-05853-9
25
Massimo Pancione, Nicola Forte, Alessandra Fucci, Lina Sabatino, Antonio Febbraro, Arturo Di Blasi, Bruno Daniele, Domenico Parente, Vittorio Colantuoni. Prognostic role of β-catenin and p53 expression in the metastatic progression of sporadic colorectal cancer. Human Pathology 2010; 41(6) doi: 10.1016/j.humpath.2009.09.019
26
Denise G. Priolli, Thamy P. Canelloi, Camila O. Lopes, Júlio C. M. Valdívia, Natalia P. Martinez, Demetrius P. Açari, Izilda A. Cardinalli, Marcelo L. Ribeiro. Oxidative DNA damage and β-catenin expression in colorectal cancer evolution. International Journal of Colorectal Disease 2013; 28(5) doi: 10.1007/s00384-013-1688-7
27
Juan Gu, Chang-fu Cui, Li Yang, Ling Wang, Xue-hua Jiang. Emodin Inhibits Colon Cancer Cell Invasion and Migration by Suppressing Epithelial‐Mesenchymal Transition via the Wnt/β-Catenin Pathway. Oncology Research Featuring Preclinical and Clinical Cancer Therapeutics 2019; 27(2) doi: 10.3727/096504018X15150662230295
28
Haiyan Zhai, Andrew Fesler, Kristina Schee, Øystein Fodstad, Kjersti Flatmark, Jingfang Ju. Clinical Significance of Long Intergenic Noncoding RNA-p21 in Colorectal Cancer. Clinical Colorectal Cancer 2013; 12(4) doi: 10.1016/j.clcc.2013.06.003
29
SURASAK SANGKHATHAT, SAMORNMAS KANNGURN, WELAWEE CHAIYAPAN, PODCHANAPORN GRIDIST, WANWISA MANEECHAY. Wilms’ tumor 1 gene (WT1) is overexpressed and provides an oncogenic function in pediatric nephroblastomas harboring the wild-type WT1. Oncology Letters 2010; 1(4) doi: 10.3892/ol_00000109
30
Song-Yi Choi, Young Suk Jo, Song-Mei Huang, Zhe Long Liang, Jeong-Ki Min, Hyo Jeong Hong, Jin-Man Kim. L1 cell adhesion molecule as a novel independent poor prognostic factor in gallbladder carcinoma. Human Pathology 2011; 42(10) doi: 10.1016/j.humpath.2011.01.003
31
Lin Li, Shiyun Yuan, Xunping Zhao, Tao Luo. ADAMTS8 is frequently down-regulated in colorectal cancer and functions as a tumor suppressor. Biochemical and Biophysical Research Communications 2020; 524(3) doi: 10.1016/j.bbrc.2020.01.020
32
Shushan Yan, Chunjuan Yang, Jiaojiao Zhang, Wenchang Sun, Xinyi Yan, Jinke Du, Wenqing Dai, Honggang Wang, Donghua Xu. Exosomal Circ_0125473 Drives Macrophages Polarization Toward M2 Through miR-5787/Wnt1/β-Catenin Signaling Pathway in Colorectal Cancer. SSRN Electronic Journal 2021;  doi: 10.2139/ssrn.3893778
33
Walawee Chaiyapan, Surasak Sangkhathat, Samornmas Kanngurn, Monlika Phukaoloun, Piyawan Chiengkriwate, Sakda Patrapinyokul. Immunohistological evidence for Wnt-signaling activation in Peutz-Jeghers polyposis. Pediatric Surgery International 2010; 26(2) doi: 10.1007/s00383-009-2547-z
34
Ana Sebio, Michael Kahn, Heinz-Josef Lenz. The potential of targeting Wnt/β-catenin in colon cancer. Expert Opinion on Therapeutic Targets 2014; 18(6) doi: 10.1517/14728222.2014.906580
35
Seung-Hyun Lee, Hyun-Jeong Kang, Byung-Kwon Ahn, Sung-Uhn Baek, Hee-Kyung Chang, Nham-Gun Oh, Mee-Young Sol, Do-Youn Park. Clinicopathologic Factors for Prediction of Lymph Node Metastasis in Submucosally Invasive Colorectal Carcinoma. Journal of the Korean Surgical Society 2011; 80(2) doi: 10.4174/jkss.2011.80.2.111
36
SEBASTIAN KRAUS, CHRISTIAN VAY, STEPHAN BALDUS, WOLFRAM T. KNOEFEL, NIKOLAS H. STOECKLEIN, DANIEL VALLBOHMER. Expression of wingless-type mouse mammary tumor virus integration site family pathway effectors in lymphatic and hepatic metastases of patients with colorectal cancer: Associations with the primary tumor. Oncology Letters 2015; 10(2) doi: 10.3892/ol.2015.3291
37
Zhongyuan Wang, Liang Zhou, Yanpeng Xiong, Shubin Yu, Huan Li, Jiaoyang Fan, Fan Li, Zijie Su, Jiaxing Song, Qi Sun, Shan‐Shan Liu, Yuqing Xia, Liang Zhao, Shiyue Li, Fang Guo, Peng Huang, Dennis A. Carson, Desheng Lu. Salinomycin exerts anti‐colorectal cancer activity by targeting the β‐catenin/T‐cell factor complex. British Journal of Pharmacology 2019; 176(17) doi: 10.1111/bph.14770