Mesenchymal to Epithelial Transition Induced by Reprogramming Factors Attenuates the Malignancy of Cancer Cells

Epithelial to mesenchymal transition (EMT) is a biological process of metastatic cancer. However, an effective anticancer therapy that directly targets the EMT program has not yet been discovered. Recent studies have indicated that mesenchymal to epithelial transition (MET), the reverse phenomenon of EMT, is observed in fibroblasts during the generation of induced pluripotent stem cells. In the present study, we investigated the effects of reprogramming factors (RFs) on squamous cell carcinoma (SCC) cells. RFs-introduced cancer cells (RICs) demonstrated the enhanced epithelial characteristics in morphology with altered expression of mRNA and microRNAs. The motility and invasive activities of RICs in vitro were significantly reduced. Furthermore, xenografts of RICs exhibited no lymph node metastasis, whereas metastasis was detected in parental SCC-inoculated mice. Thus, we concluded that RICs regained epithelial properties through MET and showed reduced cancer malignancy in vitro and in vivo. Therefore, the understanding of the MET process in cancer cells by introduction of RFs may lead to the designing of a novel anticancer strategy.

[1]  T. Seufferlein,et al.  The role of pluripotency factors to drive stemness in gastrointestinal cancer. , 2016, Stem cell research.

[2]  James E. Verdone,et al.  Polyclonal breast cancer metastases arise from collective dissemination of keratin 14-expressing tumor cell clusters , 2016, Proceedings of the National Academy of Sciences.

[3]  S. Yamanaka,et al.  A developmental framework for induced pluripotency , 2015, Development.

[4]  L. S. Oliveira,et al.  Small RNAs in metastatic and non-metastatic oral squamous cell carcinoma , 2015, BMC Medical Genomics.

[5]  Marian Hajduch,et al.  Diagnostic and prognostic potential of miR-21, miR-29c, miR-148 and miR-203 in adenocarcinoma and squamous cell carcinoma of esophagus , 2015, Diagnostic Pathology.

[6]  Naser Asl Aminabadi,et al.  MicroRNAs as prognostic molecular signatures in human head and neck squamous cell carcinoma: a systematic review and meta-analysis. , 2015, Oral oncology.

[7]  Stephen T. C. Wong,et al.  The osteogenic niche promotes early-stage bone colonization of disseminated breast cancer cells. , 2015, Cancer cell.

[8]  F. Watt,et al.  Rewiring of an Epithelial Differentiation Factor, miR-203, to Inhibit Human Squamous Cell Carcinoma Metastasis , 2014, Cell reports.

[9]  M. Toyoda,et al.  Embryonic Stem Cells / Induced Pluripotent Stem ( iPS ) Cells RemovalofReprogrammingTransgenes Improves the Tissue Reconstitution Potential of Keratinocytes Generated From Human Induced Pluripotent Stem Cells , 2014 .

[10]  Sridhar Ramaswamy,et al.  Circulating Tumor Cell Clusters Are Oligoclonal Precursors of Breast Cancer Metastasis , 2014, Cell.

[11]  A. Díaz-López,et al.  Cancer Management and Research Dovepress Role of Microrna in Epithelial to Mesenchymal Transition and Metastasis and Clinical Perspectives , 2022 .

[12]  Yibin Kang,et al.  Multilayer control of the EMT master regulators , 2014, Oncogene.

[13]  Ming Liu,et al.  MiR-203 is downregulated in laryngeal squamous cell carcinoma and can suppress proliferation and induce apoptosis of tumours , 2014, Tumor Biology.

[14]  Y. Xi,et al.  MiR-200, a new star miRNA in human cancer. , 2014, Cancer letters.

[15]  Samy Lamouille,et al.  Molecular mechanisms of epithelial–mesenchymal transition , 2014, Nature Reviews Molecular Cell Biology.

[16]  Ayla Orang,et al.  Insights into the diverse roles of miR-205 in human cancers. , 2014, Asian Pacific journal of cancer prevention : APJCP.

[17]  R. Matkowski,et al.  Circulating Tumor , 2014 .

[18]  Andrew J. Ewald,et al.  Collective Invasion in Breast Cancer Requires a Conserved Basal Epithelial Program , 2013, Cell.

[19]  Jing Yang,et al.  Epithelial–mesenchymal plasticity in carcinoma metastasis , 2013, Genes & development.

[20]  P. Itin,et al.  MicroRNA expression differs in cutaneous squamous cell carcinomas and healthy skin of immunocompetent individuals , 2013, Experimental dermatology.

[21]  Samy Lamouille,et al.  Regulation of epithelial-mesenchymal and mesenchymal-epithelial transitions by microRNAs. , 2013, Current opinion in cell biology.

[22]  Jie Chen,et al.  Critical regulation of miR-200/ZEB2 pathway in Oct4/Sox2-induced mesenchymal-to-epithelial transition and induced pluripotent stem cell generation , 2013, Proceedings of the National Academy of Sciences.

[23]  G. Berx,et al.  Regulatory networks defining EMT during cancer initiation and progression , 2013, Nature Reviews Cancer.

[24]  M. Terry,et al.  Terminal differentiation and loss of tumorigenicity of human cancers via pluripotency based reprogramming , 2012, Oncogene.

[25]  Tao He,et al.  Normal and disease-related biological functions of Twist1 and underlying molecular mechanisms , 2011, Cell Research.

[26]  H. Aburatani,et al.  Generation of induced pluripotent stem cells from primary chronic myelogenous leukemia patient samples. , 2010, Blood.

[27]  Helmut Schaider,et al.  Transcriptional activation of ZEB1 by Slug leads to cooperative regulation of the epithelial-mesenchymal transition-like phenotype in melanoma. , 2011, The Journal of investigative dermatology.

[28]  M. Cleary,et al.  HIF induces human embryonic stem cell markers in cancer cells. , 2011, Cancer research.

[29]  Jia Liu,et al.  Twist2 contributes to breast cancer progression by promoting an epithelial–mesenchymal transition and cancer stem-like cell self-renewal , 2011, Oncogene.

[30]  Bernadett Papp,et al.  Reprogramming to pluripotency: stepwise resetting of the epigenetic landscape , 2011, Cell Research.

[31]  三吉 範克 Defined factors induce reprogramming of gastrointestinal cancer cells , 2011 .

[32]  J. Wrana,et al.  Functional genomics reveals a BMP-driven mesenchymal-to-epithelial transition in the initiation of somatic cell reprogramming. , 2010, Cell stem cell.

[33]  Jialiang Liang,et al.  A mesenchymal-to-epithelial transition initiates and is required for the nuclear reprogramming of mouse fibroblasts. , 2010, Cell stem cell.

[34]  R. Jaenisch,et al.  Generation of iPSCs from cultured human malignant cells. , 2010, Blood.

[35]  R. Keri,et al.  Krüppel-like Factor 4 Inhibits Epithelial-to-Mesenchymal Transition through Regulation of E-cadherin Gene Expression* , 2010, The Journal of Biological Chemistry.

[36]  J. Utikal,et al.  Sox2 is dispensable for the reprogramming of melanocytes and melanoma cells into induced pluripotent stem cells , 2009, Journal of Cell Science.

[37]  A. Bradley,et al.  Generation of transgene-free induced pluripotent mouse stem cells by the piggyBac transposon , 2009, Nature Methods.

[38]  T. Brabletz,et al.  A reciprocal repression between ZEB1 and members of the miR-200 family promotes EMT and invasion in cancer cells , 2008, EMBO reports.

[39]  Kohei Miyazono,et al.  Differential Regulation of Epithelial and Mesenchymal Markers by δEF1 Proteins in Epithelial–Mesenchymal Transition Induced by TGF-β , 2007 .

[40]  A. Cano,et al.  Snail silencing effectively suppresses tumour growth and invasiveness , 2007, Oncogene.

[41]  Kohei Miyazono,et al.  Differential regulation of epithelial and mesenchymal markers by deltaEF1 proteins in epithelial mesenchymal transition induced by TGF-beta. , 2007, Molecular biology of the cell.

[42]  M. Fraga,et al.  The transcription factor Slug represses E-cadherin expression and induces epithelial to mesenchymal transitions: a comparison with Snail and E47 repressors , 2003, Journal of Cell Science.

[43]  E. Fearon,et al.  The SLUG zinc-finger protein represses E-cadherin in breast cancer. , 2002, Cancer research.

[44]  前川 謙一 Inhibition of cervical lymph node metastasis by marimastat (BB-2516) in an orthotopic oral squamous cell carcinoma implantation model , 2002 .

[45]  G. Berx,et al.  The two-handed E box binding zinc finger protein SIP1 downregulates E-cadherin and induces invasion. , 2001, Molecular cell.

[46]  N. Kamata,et al.  Reverse correlation of E-cadherin and snail expression in oral squamous cell carcinoma cells in vitro. , 2001, Oral oncology.

[47]  S. Frisch,et al.  Evidence for a function of CtBP in epithelial gene regulation and anoikis , 2000, Oncogene.

[48]  Dai,et al.  Platelet activation. , 2020, Arteriosclerosis.

[49]  M. Nagayama,et al.  Simultaneous production of G- and M-CSF by an oral cancer cell line and the synergistic effects on associated leucocytosis. , 1995, European journal of cancer. Part B, Oral oncology.

[50]  N. Tsuchida,et al.  Activation of oncogenes in human oral cancer cells: a novel codon 13 mutation of c-H-ras-1 and concurrent amplifications of c-erbB-1 and c-myc. , 1989, Oncogene.