Stem cells in liver diseases and cancer: Recent advances on the path to new therapies

被引:84
作者
Rountree, C. Bart [1 ]
Mishra, Lopa [2 ]
Willenbring, Holger [3 ,4 ]
机构
[1] Penn State Coll Med, Dept Pediat & Pharmacol, Hershey, PA 17033 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Gastroenterol Hepatol & Nutr, Houston, TX 77030 USA
[3] Univ Calif San Francisco, Ctr Liver, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Dept Surg, Div Transplantat, Eli & Edythe Broad Ctr Regenerat Med & Stem Cell, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
HEPATOCELLULAR-CARCINOMA CELLS; HEPATOCYTE-LIKE CELLS; EPIGENETIC REGULATION; PROGENITOR CELLS; DIFFERENTIATION; BETA; MICE; HEPATOCARCINOGENESIS; REGENERATION; EXPRESSION;
D O I
10.1002/hep.24762
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Stem cells have potential for therapy of liver diseases, but may also be involved in the formation of liver cancer. Recently, the American Association for the Study of Liver Diseases Henry M. and Lillian Stratton Basic Research Single Topic Conference Stem Cells in Liver Diseases and Cancer: Discovery and Promise brought together a diverse group of investigators to define the status of research on stem cells and cancer stem cells in the liver and identify problems and solutions on the path to clinical translation. This report summarizes the outcomes of the conference and provides an update on recent research advances. Progress in liver stem cell research includes isolation of primary liver progenitor cells (LPCs), directed hepatocyte differentiation of primary LPCs and pluripotent stem cells, findings of transdifferentiation, disease-specific considerations for establishing a therapeutically effective cell mass, and disease modeling in cell culture. Tumor-initiating stem-like cells (TISCs) that emerge during chronic liver injury share the expression of signaling pathways, including those organized around transforming growth factor beta and beta-catenin, and surface markers with normal LPCs. Recent investigations of the role of TISCs in hepatocellular carcinoma have provided insight into the transcriptional and post-transcriptional regulation of hepatocarcinogenesis. Targeted chemotherapies for TISC are in development as a means to overcome cellular resistance and mechanisms driving disease progression in liver cancer. (HEPATOLOGY 2012;55:298306)
引用
收藏
页码:298 / 306
页数:9
相关论文
共 77 条
[1]   Prospective identification of tumorigenic breast cancer cells [J].
Al-Hajj, M ;
Wicha, MS ;
Benito-Hernandez, A ;
Morrison, SJ ;
Clarke, MF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (07) :3983-3988
[2]   Progenitor-Derived Hepatocellular Carcinoma Model in the Rat [J].
Andersen, Jesper B. ;
Loi, Roberto ;
Perra, Andrea ;
Factor, Valentina M. ;
Ledda-Columbano, Giovanna M. ;
Columbano, Amedeo ;
Thorgeirsson, Snorri S. .
HEPATOLOGY, 2010, 51 (04) :1401-1409
[3]   Transforming Growth Factor-β Adaptor, β2-Spectrin, Modulates Cyclin Dependent Kinase 4 to Reduce Development of Hepatocellular Cancer [J].
Baek, Hye Jung ;
Pishvaian, Michael J. ;
Tang, Yi ;
Kim, Tae Hyun ;
Yang, Shaoxian ;
El Zouhairi, Majed ;
Mendelson, Jon ;
Shetty, Kirti ;
Kallakury, Bhaskar ;
Berry, Deborah L. ;
Shin, Kyung Hwan ;
Mishra, Bibhuti ;
Reddy, E. Premkumar ;
Kim, Sang Soo ;
Mishra, Lopa .
HEPATOLOGY, 2011, 53 (05) :1676-1684
[4]   Targeted Inhibition of Kinases in Cancer Therapy [J].
Baker, Stacey J. ;
Reddy, E. Premkumar .
MOUNT SINAI JOURNAL OF MEDICINE, 2010, 77 (06) :573-586
[5]   The Use of Whole Organ Decellularization for the Generation of a Vascularized Liver Organoid [J].
Baptista, Pedro M. ;
Siddiqui, Mohummad M. ;
Lozier, Genevieve ;
Rodriguez, Sergio R. ;
Atala, Anthony ;
Soker, Shay .
HEPATOLOGY, 2011, 53 (02) :604-617
[6]   Differentiation and Transplantation of Human Embryonic Stem Cell-Derived Hepatocytes [J].
Basma, Hesham ;
Soto-Gutierrez, Alejandro ;
Yannam, Govardhana Rao ;
Liu, Liping ;
Ito, Ryotaro ;
Yamamoto, Toshiyuki ;
Ellis, Ewa ;
Carson, Steven D. ;
Sato, Shintaro ;
Chen, Yong ;
Muirhead, David ;
Navarro-Alvarez, Nalu ;
Wong, Ronald J. ;
Roy-Chowdhury, Jayanta ;
Platt, Jeffrey L. ;
Mercer, David F. ;
Miller, John D. ;
Strom, Stephen C. ;
Kobayashi, Naoya ;
Fox, Ira J. .
GASTROENTEROLOGY, 2009, 136 (03) :990-999
[7]   EZH2 Promotes Expansion of Breast Tumor Initiating Cells through Activation of RAF1-β-Catenin Signaling [J].
Chang, Chun-Ju ;
Yang, Jer-Yen ;
Xia, Weiya ;
Chen, Chun-Te ;
Xie, Xiaoming ;
Chao, Chi-Hong ;
Woodward, Wendy A. ;
Hsu, Jung-Mao ;
Hortobagyi, Gabriel N. ;
Hung, Mien-Chie .
CANCER CELL, 2011, 19 (01) :86-100
[8]   EZH2-Mediated Concordant Repression of Wnt Antagonists Promotes β-Catenin-Dependent Hepatocarcinogenesis [J].
Cheng, Alfred S. L. ;
Lau, Suki S. ;
Chen, Yangchao ;
Kondo, Yutaka ;
Li, May S. ;
Feng, Hai ;
Ching, Arthur K. ;
Cheung, Kin F. ;
Wong, Hoi K. ;
Tong, Joanna H. ;
Jin, Hongchuan ;
Choy, Kwong W. ;
Yu, Jun ;
To, Ka F. ;
Wong, Nathalie ;
Huang, Tim H. -M. ;
Sung, Joseph J. Y. .
CANCER RESEARCH, 2011, 71 (11) :4028-4039
[9]   Side population purified from hepatocellular carcinoma cells harbors cancer stem cell-like properties [J].
Chiba, Tetsuhiro ;
Kita, Kaoru ;
Zheng, Yun-Wen ;
Yokosuka, Osamu ;
Saisho, Hiromitsu ;
Iwama, Atsushi ;
Nakauchi, Hiromitsu ;
Taniguchi, Hideki .
HEPATOLOGY, 2006, 44 (01) :240-251
[10]   Vitamin Analogues in Chemoprevention of Hepatocellular Carcinoma After Resection or Ablation-A Systematic Review and Meta-analysis [J].
Chu, Kai-Jian ;
Lai, Eric C. H. ;
Yao, Xiao-Ping ;
Zhang, Hong-Wei ;
Lau, Wan Yee ;
Fu, Xiao-Hui ;
Lu, Chong-De ;
Shi, Jie ;
Cheng, Shu-Qun .
ASIAN JOURNAL OF SURGERY, 2010, 33 (03) :120-126