Association of Preoperative NANOG-Positive Circulating Tumor Cell Levels With Recurrence of Hepatocellular Carcinoma

Cancer stem cells (CSCs) and Circulating tumor cells (CTCs) have been proposed as fundamental causes for the recurrence of hepatocellular carcinoma (HCC). CTCs isolated from patients with HCC illustrate a unique Nanog expression profile analysis. The aim of this study was to enhance the prediction o...

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Published inFrontiers in oncology Vol. 11; p. 601668
Main Authors Lei, Yongrong, Wang, Xishu, Sun, Heng, Fu, Yuna, Tian, Yichen, Yang, Ludi, Wang, Jianhua, Xia, Feng
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 27.05.2021
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ISSN2234-943X
2234-943X
DOI10.3389/fonc.2021.601668

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Abstract Cancer stem cells (CSCs) and Circulating tumor cells (CTCs) have been proposed as fundamental causes for the recurrence of hepatocellular carcinoma (HCC). CTCs isolated from patients with HCC illustrate a unique Nanog expression profile analysis. The aim of this study was to enhance the prediction of recurrence and prognosis of the CTC phenotype in patients with HCC by combining Nanog expression into a combined forecasting model. We collected 320 blood samples from 160 patients with HCC cancer before surgery and used CanPatrol™ CTC enrichment technology and in situ hybridization (ISH) to enrich and detect CTCs and CSCs. Nanog expression in all CTCs was also determined. In addition, RT-PCR and immunohistochemistry were used to study the expression of Nanog, E-Cadherin, and N-Cadherin in liver cancer tissues and to conduct clinical correlation studies. The numbers of CTCs and CTCs were strongly correlated with postoperative HCC recurrence (CTC number (P = 0.03), the total number of mixed CTCS (P = 0.02), and Nanog> 6.7 (P = 0.001), with Nanog > 6.7 (P = 0.0003, HR = 2.33) being the most crucial marker. There are significant differences in the expression of Nanog on different types of CTC: most Epithelial CTCs do not express Nanog, while most of Mixed CTC and Mesenchymal CTC express Nanog, and their positive rates are 38.7%, 66.7%, and 88.7%, respectively, (P=0.0001). Moreover, both CTC (≤/> 13.3) and Nanog (≤/>6.7) expression were significantly correlated with BCLC stage, vascular invasion, tumor size, and Hbv-DNA (all P < 0.05). In the young group and the old group, patients with higher Nanog expression had a higher recurrence rate. (P < 0.001). The number of Nanog-positive cells showed positive correlation with the poor prognosis of HCC patients. The detection and analysis of CTC markers (EpCAM and CK8, 18, CD45 Vimentin,Twist and 19) and CSCs markers (NANOG) are of great value in the evaluation of tumor progression.
AbstractList Cancer stem cells (CSCs) and Circulating tumor cells (CTCs) have been proposed as fundamental causes for the recurrence of hepatocellular carcinoma (HCC). CTCs isolated from patients with HCC illustrate a unique Nanog expression profile analysis. The aim of this study was to enhance the prediction of recurrence and prognosis of the CTC phenotype in patients with HCC by combining Nanog expression into a combined forecasting model.BACKGROUNDCancer stem cells (CSCs) and Circulating tumor cells (CTCs) have been proposed as fundamental causes for the recurrence of hepatocellular carcinoma (HCC). CTCs isolated from patients with HCC illustrate a unique Nanog expression profile analysis. The aim of this study was to enhance the prediction of recurrence and prognosis of the CTC phenotype in patients with HCC by combining Nanog expression into a combined forecasting model.We collected 320 blood samples from 160 patients with HCC cancer before surgery and used CanPatrol™ CTC enrichment technology and in situ hybridization (ISH) to enrich and detect CTCs and CSCs. Nanog expression in all CTCs was also determined. In addition, RT-PCR and immunohistochemistry were used to study the expression of Nanog, E-Cadherin, and N-Cadherin in liver cancer tissues and to conduct clinical correlation studies.SUBJECTS MATERIALS AND METHODSWe collected 320 blood samples from 160 patients with HCC cancer before surgery and used CanPatrol™ CTC enrichment technology and in situ hybridization (ISH) to enrich and detect CTCs and CSCs. Nanog expression in all CTCs was also determined. In addition, RT-PCR and immunohistochemistry were used to study the expression of Nanog, E-Cadherin, and N-Cadherin in liver cancer tissues and to conduct clinical correlation studies.The numbers of EpCAM mRNA+ CTCs and Nanog mRNA+ CTCs were strongly correlated with postoperative HCC recurrence (CTC number (P = 0.03), the total number of mixed CTCS (P = 0.02), and Nanog> 6.7 (P = 0.001), with Nanog > 6.7 (P = 0.0003, HR = 2.33) being the most crucial marker. There are significant differences in the expression of Nanog on different types of CTC: most Epithelial CTCs do not express Nanog, while most of Mixed CTC and Mesenchymal CTC express Nanog, and their positive rates are 38.7%, 66.7%, and 88.7%, respectively, (P=0.0001). Moreover, both CTC (≤/> 13.3) and Nanog (≤/>6.7) expression were significantly correlated with BCLC stage, vascular invasion, tumor size, and Hbv-DNA (all P < 0.05). In the young group and the old group, patients with higher Nanog expression had a higher recurrence rate. (P < 0.001).RESULTSThe numbers of EpCAM mRNA+ CTCs and Nanog mRNA+ CTCs were strongly correlated with postoperative HCC recurrence (CTC number (P = 0.03), the total number of mixed CTCS (P = 0.02), and Nanog> 6.7 (P = 0.001), with Nanog > 6.7 (P = 0.0003, HR = 2.33) being the most crucial marker. There are significant differences in the expression of Nanog on different types of CTC: most Epithelial CTCs do not express Nanog, while most of Mixed CTC and Mesenchymal CTC express Nanog, and their positive rates are 38.7%, 66.7%, and 88.7%, respectively, (P=0.0001). Moreover, both CTC (≤/> 13.3) and Nanog (≤/>6.7) expression were significantly correlated with BCLC stage, vascular invasion, tumor size, and Hbv-DNA (all P < 0.05). In the young group and the old group, patients with higher Nanog expression had a higher recurrence rate. (P < 0.001).The number of Nanog-positive cells showed positive correlation with the poor prognosis of HCC patients. The detection and analysis of CTC markers (EpCAM and CK8, 18, CD45 Vimentin,Twist and 19) and CSCs markers (NANOG) are of great value in the evaluation of tumor progression.CONCLUSIONSThe number of Nanog-positive cells showed positive correlation with the poor prognosis of HCC patients. The detection and analysis of CTC markers (EpCAM and CK8, 18, CD45 Vimentin,Twist and 19) and CSCs markers (NANOG) are of great value in the evaluation of tumor progression.
Cancer stem cells (CSCs) and Circulating tumor cells (CTCs) have been proposed as fundamental causes for the recurrence of hepatocellular carcinoma (HCC). CTCs isolated from patients with HCC illustrate a unique Nanog expression profile analysis. The aim of this study was to enhance the prediction of recurrence and prognosis of the CTC phenotype in patients with HCC by combining Nanog expression into a combined forecasting model. We collected 320 blood samples from 160 patients with HCC cancer before surgery and used CanPatrol™ CTC enrichment technology and in situ hybridization (ISH) to enrich and detect CTCs and CSCs. Nanog expression in all CTCs was also determined. In addition, RT-PCR and immunohistochemistry were used to study the expression of Nanog, E-Cadherin, and N-Cadherin in liver cancer tissues and to conduct clinical correlation studies. The numbers of CTCs and CTCs were strongly correlated with postoperative HCC recurrence (CTC number (P = 0.03), the total number of mixed CTCS (P = 0.02), and Nanog> 6.7 (P = 0.001), with Nanog > 6.7 (P = 0.0003, HR = 2.33) being the most crucial marker. There are significant differences in the expression of Nanog on different types of CTC: most Epithelial CTCs do not express Nanog, while most of Mixed CTC and Mesenchymal CTC express Nanog, and their positive rates are 38.7%, 66.7%, and 88.7%, respectively, (P=0.0001). Moreover, both CTC (≤/> 13.3) and Nanog (≤/>6.7) expression were significantly correlated with BCLC stage, vascular invasion, tumor size, and Hbv-DNA (all P < 0.05). In the young group and the old group, patients with higher Nanog expression had a higher recurrence rate. (P < 0.001). The number of Nanog-positive cells showed positive correlation with the poor prognosis of HCC patients. The detection and analysis of CTC markers (EpCAM and CK8, 18, CD45 Vimentin,Twist and 19) and CSCs markers (NANOG) are of great value in the evaluation of tumor progression.
BackgroundCancer stem cells (CSCs) and Circulating tumor cells (CTCs) have been proposed as fundamental causes for the recurrence of hepatocellular carcinoma (HCC). CTCs isolated from patients with HCC illustrate a unique Nanog expression profile analysis. The aim of this study was to enhance the prediction of recurrence and prognosis of the CTC phenotype in patients with HCC by combining Nanog expression into a combined forecasting model.Subjects, Materials, and MethodsWe collected 320 blood samples from 160 patients with HCC cancer before surgery and used CanPatrol™ CTC enrichment technology and in situ hybridization (ISH) to enrich and detect CTCs and CSCs. Nanog expression in all CTCs was also determined. In addition, RT-PCR and immunohistochemistry were used to study the expression of Nanog, E-Cadherin, and N-Cadherin in liver cancer tissues and to conduct clinical correlation studies.ResultsThe numbers of EpCAM mRNA+ CTCs and Nanog mRNA+ CTCs were strongly correlated with postoperative HCC recurrence (CTC number (P = 0.03), the total number of mixed CTCS (P = 0.02), and Nanog> 6.7 (P = 0.001), with Nanog > 6.7 (P = 0.0003, HR = 2.33) being the most crucial marker. There are significant differences in the expression of Nanog on different types of CTC: most Epithelial CTCs do not express Nanog, while most of Mixed CTC and Mesenchymal CTC express Nanog, and their positive rates are 38.7%, 66.7%, and 88.7%, respectively, (P=0.0001). Moreover, both CTC (≤/> 13.3) and Nanog (≤/>6.7) expression were significantly correlated with BCLC stage, vascular invasion, tumor size, and Hbv-DNA (all P < 0.05). In the young group and the old group, patients with higher Nanog expression had a higher recurrence rate. (P < 0.001).ConclusionsThe number of Nanog-positive cells showed positive correlation with the poor prognosis of HCC patients. The detection and analysis of CTC markers (EpCAM and CK8, 18, CD45 Vimentin,Twist and 19) and CSCs markers (NANOG) are of great value in the evaluation of tumor progression.
Author Lei, Yongrong
Wang, Jianhua
Yang, Ludi
Sun, Heng
Tian, Yichen
Xia, Feng
Wang, Xishu
Fu, Yuna
AuthorAffiliation 2 Key Laboratory of Hepatobiliary and Pancreatic Surgery, Institute of Hepatobiliary Surgery, Southwest Hospital, the First Hospital Affiliated to AMU (Southwest Hospital) , Chongqing , China
1 Key Laboratory of Biorheological Science and Technology, Ministry of Education, College of Bioengineering, Chongqing University , Chongqing , China
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Cites_doi 10.1002/hep.24199
10.1634/theoncologist.2018-0697
10.1158/1535-7163.mct-18-0584
10.1016/j.cmet.2018.11.004
10.7150/thno.28745
10.1002/hep.27721
10.1007/s12072-016-9732-7
10.1186/s12943-019-0976-4
10.1016/j.cell.2008.03.027
10.1373/clinchem.2019.308965
10.1073/pnas.1508541113
10.1515/cclm-2013-0558
10.1016/j.semcancer.2017.02.011
10.3390/cells9020386
10.1158/2159-8290.cd-18-1285
10.1186/s13046-019-1429-z
10.1016/j.bbi.2016.08.016
10.1158/0008-5472.can-17-2459
10.1007/s10911-020-09443-6
10.3390/cancers11091274
10.1038/nrc1740
10.1016/j.stem.2015.02.015
10.1016/j.mam.2019.06.002
10.1158/0008-5472.can-18-0650
10.1002/hep.25745
10.1038/nrclinonc.2016.128
10.1016/j.bbcan.2019.188315
10.1016/j.nano.2019.102106
10.1073/pnas.1102454108
10.1038/s41598-017-13501-1
10.3389/fonc.2019.01015
10.1158/0008-5472.can-19-1110
10.1021/acsami.9b18410
10.1158/2159-8290.cd-19-0384
10.3390/cancers11010022
10.1111/hepr.13433
10.1634/theoncologist.2018-0784
10.1002/jcb.28128
10.1158/0008-5472.can-18-2376
10.1038/nature12628
10.1158/1078-0432.ccr-17-1063
10.1158/0008-5472.can-18-0644
10.1073/pnas.1907904116
10.3748/wjg.v21.i47.13259
10.1126/scitranslmed.aat5857
10.1001/jamasurg.2018.2721
10.3389/fonc.2018.00063
10.1038/s41598-019-43572-1
10.1016/j.cca.2017.11.037
10.1136/gut.2008.176271
10.7150/thno.29271
10.1021/jacs.8b12872
10.1016/j.mam.2019.07.008
10.7150/thno.37717
10.1016/j.ccr.2006.06.016
10.1158/2159-8290.cd-12-0312
10.1016/j.cell.2014.07.013
10.3892/etm.2016.3283
10.1186/s13046-017-0559-4
10.1101/cshperspect.a036905
10.1177/1758835918816287
10.5483/BMBRep.2015.48.3.047
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Keywords recurrence
cancer stem cells
circulating tumor cells
epithelial-mesenchymal
hepatocellular carcinoma
Language English
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Edited by: Antonella Zannetti, Institute of Biostructure and Bioimaging (CNR), Italy
This article was submitted to Molecular and Cellular Oncology, a section of the journal Frontiers in Oncology
Reviewed by: Anca Maria Cimpean, Victor Babes University of Medicine and Pharmacy, Romania; Rinaldo Pellicano, Molinette Hospital, Italy
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References May (B9) 2018; 8
Pu (B45) 2020; 25
Cai (B61) 2018
Wang (B32) 2019; 141
Shan (B43) 2012; 56
Chaffer (B26) 2011; 108
Liu (B51) 2018; 78
Kao (B57) 2019; 79
Qi (B38) 2018; 78
Yang (B62) 2010; 59
Tan (B6) 2019; 24
Wei (B7) 2019; 18
Saga (B18) 2019; 38
Budhu (B53) 2006; 10
Bjerkvig (B56) 2005; 5
Galanzha (B50) 2019; 11
Liang (B29) 2018; 477
Buderath (B8) 2019; 9
Räsänen (B23) 2012; 2
Pu (B42) 2020; 25
Fan (B60) 2018; 11
Plaks (B64) 2015; 16
Gener (B12) 2020; 24
Cernigliaro (B27) 2020; 9
Bruix (B36) 2011; 53
Celià-Terrassa (B21) 2020; 10
Marcuello (B46) 2019; 69
Wu (B24) 2019; 29
Peitzsch (B1) 2017; 44
Cheung (B5) 2016; 113
Nicolazzo (B16) 2019; 24
Cao (B30) 2019; 9
Sun (B54) 2018; 24
Varillas (B33) 2019; 9
Yang (B39) 2019; 65
Najim (B13) 2019; 1872
Wang (B59) 2018; 10
Papadaki (B28) 2019; 18
Wu (B40) 2014; 52
Lee (B55) 2017; 7
Peiffer (B19) 2019; 79
Chen (B35) 2019; 9
Martin (B10) 2017; 14
Khoo (B15) 2019; 11
Li (B41) 2015; 21
Lim (B14) 2019; 116
Lee (B52) 2015; 48
Mani (B22) 2008; 133
Sun (B34) 2018; 24
Lee (B25) 2015; 61
Xie (B48) 2016; 12
Aceto (B4) 2014; 158
Cortés-Hernández (B3) 2020; 72
Lin (B20) 2019; 9
Huan (B17) 2017; 59
Rodrigues (B31) 2019; 9
Klein (B2) 2013; 501
Liu (B37) 2016; 10
Wu (B49) 2019; 11
Vishnoi (B11) 2018; 78
Liu (B47) 2020; 50
Huan (B44) 2017; 36
Klotz (B58) 2020; 10
Li (B63) 2018; 153
39050582 - Front Oncol. 2024 Jul 10;14:1438731. doi: 10.3389/fonc.2024.1438731
References_xml – volume: 53
  year: 2011
  ident: B36
  article-title: Management of Hepatocellular Carcinoma: An Update
  publication-title: Hepatology
  doi: 10.1002/hep.24199
– volume: 24
  start-page: e1044–54
  year: 2019
  ident: B6
  article-title: Incorporating MicroRNA into Molecular Phenotypes of Circulating Tumor Cells Enhances the Prognostic Accuracy for Patients with Metastatic Breast Cancer
  publication-title: Oncologist
  doi: 10.1634/theoncologist.2018-0697
– volume: 18
  year: 2019
  ident: B28
  article-title: Circulating Tumor Cells with Stemness and Epithelial-to-Mesenchymal Transition Features Are Chemoresistant and Predictive of Poor Outcome in Metastatic Breast Cancer
  publication-title: Mol Cancer Ther
  doi: 10.1158/1535-7163.mct-18-0584
– volume: 29
  start-page: 993
  year: 2019
  ident: B24
  article-title: Epithelial-Mesenchymal Transition Directs Stem Cell Polarity via Regulation of Mitofusin
  publication-title: Cell Metab
  doi: 10.1016/j.cmet.2018.11.004
– volume: 9
  year: 2019
  ident: B33
  article-title: Microfluidic Isolation of Circulating Tumor Cells and Cancer Stem-Like Cells from Patients with Pancreatic Ductal Adenocarcinoma
  publication-title: Theranostics
  doi: 10.7150/thno.28745
– volume: 61
  year: 2015
  ident: B25
  article-title: Interaction of Tetraspan(in) TM4SF5 With CD44 Promotes Self-Renewal and Circulating Capacities of Hepatocarcinoma Cells
  publication-title: Hepatology
  doi: 10.1002/hep.27721
– volume: 10
  year: 2016
  ident: B37
  article-title: An Improved Strategy to Detect the Epithelial-Mesenchymal Transition Process in Circulating Tumor Cells in Hepatocellular Carcinoma Patients
  publication-title: Hepatol Int
  doi: 10.1007/s12072-016-9732-7
– volume: 18
  start-page: 64
  year: 2019
  ident: B7
  article-title: Crosstalk Between Cancer Cells and Tumor Associated Macrophages Is Required For Mesenchymal Circulating Tumor Cell-Mediated Colorectal Cancer Metastasis
  publication-title: Mol Cancer
  doi: 10.1186/s12943-019-0976-4
– volume: 133
  year: 2008
  ident: B22
  article-title: The epithelial-mesenchymal transition generates cells with properties of stem cells
  publication-title: Cell
  doi: 10.1016/j.cell.2008.03.027
– volume: 65
  year: 2019
  ident: B39
  article-title: A Novel Online Calculator Based on Serum Biomarkers to Detect Hepatocellular Carcinoma Among Patients With Hepatitis B
  publication-title: Clin Chem
  doi: 10.1373/clinchem.2019.308965
– volume: 113
  year: 2016
  ident: B5
  article-title: Polyclonal Breast Cancer Metastases Arise From Collective Dissemination of Keratin 14-Expressing Tumor Cell Clusters
  publication-title: Proc Natl Acad Sci USA
  doi: 10.1073/pnas.1508541113
– volume: 52
  year: 2014
  ident: B40
  article-title: Enrichment and Enumeration of Circulating Tumor Cells by Efficient Depletion of Leukocyte Fractions
  publication-title: Clin Chem Lab Med
  doi: 10.1515/cclm-2013-0558
– volume: 44
  start-page: 10
  year: 2017
  ident: B1
  article-title: Cancer Stem Cells: The Root of Tumor Recurrence and Metastases
  publication-title: Semin Cancer Biol
  doi: 10.1016/j.semcancer.2017.02.011
– volume: 9
  year: 2020
  ident: B27
  article-title: Evolving Cell-Based and Cell-Free Clinical Strategies for Treating Severe Human Liver Diseases
  publication-title: Cells
  doi: 10.3390/cells9020386
– volume: 9
  year: 2019
  ident: B31
  article-title: Circulating Tumor Cells: Come Together, Right Now, Over Metastasis
  publication-title: Cancer Discov
  doi: 10.1158/2159-8290.cd-18-1285
– volume: 38
  start-page: 416
  year: 2019
  ident: B18
  article-title: NANOG Helps Cancer Cells Escape NK Cell Attack by Downregulating ICAM1 During Tumorigenesis
  publication-title: J Exp Clin Cancer Res
  doi: 10.1186/s13046-019-1429-z
– volume: 59
  year: 2017
  ident: B17
  article-title: Sympathetic Nervous System Promotes Hepatocarcinogenesis by Modulating Inflammation Through Activation of Alpha1-Adrenergic Receptors of Kupffer Cells
  publication-title: Brain Behav Immun
  doi: 10.1016/j.bbi.2016.08.016
– volume: 78
  year: 2018
  ident: B38
  article-title: Circulating Tumor Cells Undergoing EMT Provide a Metric for Diagnosis and Prognosis of Patients with Hepatocellular Carcinoma
  publication-title: Cancer Res
  doi: 10.1158/0008-5472.can-17-2459
– volume: 25
  start-page: 37
  year: 2020
  ident: B45
  article-title: The Novel Transcription Factor CREB3L4 Contributes to the Progression of Human Breast Carcinoma
  publication-title: J Mammary Gland Biol Neoplasia
  doi: 10.1007/s10911-020-09443-6
– volume: 11
  start-page: 1274
  year: 2019
  ident: B15
  article-title: Detection of Clinical Mesenchymal Cancer Cells from Bladder Wash Urine for Real-Time Detection and Prognosis
  publication-title: Cancers (Basel)
  doi: 10.3390/cancers11091274
– volume: 5
  start-page: 899
  year: 2005
  ident: B56
  article-title: Opinion: The Origin of the Cancer Stem Cell: Current Controversies and New Insights
  publication-title: Nat Rev Cancer
  doi: 10.1038/nrc1740
– volume: 16
  year: 2015
  ident: B64
  article-title: The Cancer Stem Cell Niche: How Essential Is the Niche in Regulating Stemness of Tumor Cells
  publication-title: Cell Stem Cell
  doi: 10.1016/j.stem.2015.02.015
– volume: 69
  year: 2019
  ident: B46
  article-title: Circulating Biomarkers For Early Detection and Clinical Management of Colorectal Cancer
  publication-title: Mol Aspects Med
  doi: 10.1016/j.mam.2019.06.002
– volume: 78
  year: 2018
  ident: B51
  article-title: Circulating Glioma Cells Exhibit Stem Cell-like Properties
  publication-title: Cancer Res
  doi: 10.1158/0008-5472.can-18-0650
– volume: 56
  year: 2012
  ident: B43
  article-title: Nanog Regulates Self-Renewal of Cancer Stem Cells Through the Insulin-Like Growth Factor Pathway in Human Hepatocellular Carcinoma
  publication-title: Hepatology
  doi: 10.1002/hep.25745
– volume: 14
  start-page: 32
  year: 2017
  ident: B10
  article-title: Does the Mobilization of Circulating Tumour Cells During Cancer Therapy Cause Metastasis
  publication-title: Nat Rev Clin Oncol
  doi: 10.1038/nrclinonc.2016.128
– volume: 1872
  year: 2019
  ident: B13
  article-title: The Association Between Type of Endocrine Therapy and Development of Estrogen Receptor-1 Mutation(s) in Patients With Hormone-Sensitive Advanced Breast Cancer: A Systematic Review and Meta-Analysis of Randomized and Non-Randomized Trials
  publication-title: Biochim Biophys Acta Rev Cancer
  doi: 10.1016/j.bbcan.2019.188315
– volume: 24
  year: 2020
  ident: B12
  article-title: Zileuton™ loaded in polymer micelles effectively reduce breast cancer circulating tumor cells and intratumoral cancer stem cells
  publication-title: Nanomedicine
  doi: 10.1016/j.nano.2019.102106
– volume: 108
  year: 2011
  ident: B26
  article-title: Normal and Neoplastic Nonstem Cells Can Spontaneously Convert to A Stem-Like State
  publication-title: Proc Natl Acad Sci USA
  doi: 10.1073/pnas.1102454108
– volume: 7
  start-page: 13201
  year: 2017
  ident: B55
  article-title: Cell-Surface Major Vault Protein Promotes Cancer Progression Through Harboring Mesenchymal and Intermediate Circulating Tumor Cells in Hepatocellular Carcinomas
  publication-title: Sci Rep
  doi: 10.1038/s41598-017-13501-1
– volume: 9
  year: 2019
  ident: B8
  article-title: Soluble Programmed Death Receptor Ligands sPD-L1 and sPD-L2 as Liquid Biopsy Markers for Prognosis and Platinum Response in Epithelial Ovarian Cancer
  publication-title: Front Oncol
  doi: 10.3389/fonc.2019.01015
– volume: 79
  year: 2019
  ident: B19
  article-title: DAXX Suppresses Tumor-Initiating Cells in Estrogen Receptor-Positive Breast Cancer Following Endocrine Therapy
  publication-title: Cancer Res
  doi: 10.1158/0008-5472.can-19-1110
– volume: 11
  year: 2019
  ident: B49
  article-title: A Dual-Targeting Functionalized Graphene Film for Rapid and Highly Sensitive Fluorescence Imaging Detection of Hepatocellular Carcinoma Circulating Tumor Cells
  publication-title: ACS Appl Mater Interf
  doi: 10.1021/acsami.9b18410
– volume: 10
  start-page: 86
  year: 2020
  ident: B58
  article-title: Circulating Tumor Cells Exhibit Metastatic Tropism and Reveal Brain Metastasis Drivers
  publication-title: Cancer Discov
  doi: 10.1158/2159-8290.cd-19-0384
– volume: 11
  start-page: 22
  year: 2018
  ident: B60
  article-title: Honokiol Eliminates Glioma/Glioblastoma Stem Cell-Like Cells Via JAK-STAT3 Signaling and Inhibits Tumor Progression by Targeting Epidermal Growth Factor Receptor
  publication-title: Cancers (Basel)
  doi: 10.3390/cancers11010022
– volume: 50
  year: 2020
  ident: B47
  article-title: Glutamine Synthetase Promotes Tumor Invasion in Hepatocellular Carcinoma Through Mediating Epithelial-Mesenchymal Transition
  publication-title: Hepatol Res
  doi: 10.1111/hepr.13433
– volume: 24
  year: 2019
  ident: B16
  article-title: Circulating Tumor Cells Identify Patients with Super-High-Risk Non-Muscle-Invasive Bladder Cancer: Updated Outcome Analysis of a Prospective Single-Center Trial
  publication-title: Oncologist
  doi: 10.1634/theoncologist.2018-0784
– year: 2018
  ident: B61
  article-title: Prognostic Evaluation of NANOG And OCT4 Expression for Posttransplantation Hepatocellular Carcinoma Recurrence
  publication-title: J Cell Biochem
  doi: 10.1002/jcb.28128
– volume: 79
  year: 2019
  ident: B57
  article-title: Regulation of miRNA Biogenesis and Histone Modification by K63-Polyubiquitinated DDX17 Controls Cancer Stem-like Features
  publication-title: Cancer Res
  doi: 10.1158/0008-5472.can-18-2376
– volume: 501
  year: 2013
  ident: B2
  article-title: Selection and Adaptation During Metastatic Cancer Progression
  publication-title: Nature
  doi: 10.1038/nature12628
– volume: 24
  year: 2018
  ident: B54
  article-title: Circulating Tumor Cells from Different Vascular Sites Exhibit Spatial Heterogeneity in Epithelial and Mesenchymal Composition and Distinct Clinical Significance in Hepatocellular Carcinoma
  publication-title: Clin Cancer Res
  doi: 10.1158/1078-0432.ccr-17-1063
– volume: 78
  year: 2018
  ident: B11
  article-title: Targeting USP7 Identifies a Metastasis-Competent State Within Bone Marrow-Resident Melanoma CTCs
  publication-title: Cancer Res
  doi: 10.1158/0008-5472.can-18-0644
– volume: 116
  year: 2019
  ident: B14
  article-title: Addressing Cellular Heterogeneity in Tumor and Circulation for Refined Prognostication
  publication-title: Proc Natl Acad Sci USA
  doi: 10.1073/pnas.1907904116
– volume: 21
  year: 2015
  ident: B41
  article-title: Evaluation of Epithelial-Mesenchymal Transitioned Circulating Tumor Cells in Patients With Resectable Gastric Cancer: Relevance to Therapy Response
  publication-title: World J Gastroenterol
  doi: 10.3748/wjg.v21.i47.13259
– volume: 11
  year: 2019
  ident: B50
  article-title: In Vivo Liquid Biopsy Using Cytophone Platform For Photoacoustic Detection of Circulating Tumor Cells in Patients With Melanoma
  publication-title: Sci Trans Med
  doi: 10.1126/scitranslmed.aat5857
– volume: 24
  year: 2018
  ident: B34
  article-title: Circulating Tumor Cells from Different Vascular Sites Exhibit Spatial Heterogeneity in Epithelial and Mesenchymal Composition and Distinct Clinical Significance in Hepatocellular Carcinoma
  publication-title: Clin Cancer Res
  doi: 10.1158/1078-0432.ccr-17-1063
– volume: 153
  start-page: e182721
  year: 2018
  ident: B63
  article-title: Association of Preoperative Antiviral Treatment With Incidences of Microvascular Invasion and Early Tumor Recurrence in Hepatitis B Virus-Related Hepatocellular Carcinoma
  publication-title: JAMA Surg
  doi: 10.1001/jamasurg.2018.2721
– volume: 25
  start-page: 37
  year: 2020
  ident: B42
  article-title: The Novel Transcription Factor CREB3L4 Contributes to the Progression of Human Breast Carcinoma
  publication-title: J Mammary Gland Biol Neoplasia
  doi: 10.1007/s10911-020-09443-6
– volume: 8
  year: 2018
  ident: B9
  article-title: In Vitro Model-Systems to Understand the Biology and Clinical Significance of Circulating Tumor Cell Clusters
  publication-title: Front Oncol
  doi: 10.3389/fonc.2018.00063
– volume: 9
  start-page: 7084
  year: 2019
  ident: B35
  article-title: Circulating Tumor Cells Undergoing EMT Are Poorly Correlated With Clinical Stages or Predictive of Recurrence in Hepatocellular Carcinoma
  publication-title: Sci Rep
  doi: 10.1038/s41598-019-43572-1
– volume: 477
  start-page: 24
  year: 2018
  ident: B29
  article-title: Prognostic and Clinicopathological Value of Nanog in Hepatocellular Carcinoma: A Meta-Analysis
  publication-title: Clin Chim Acta
  doi: 10.1016/j.cca.2017.11.037
– volume: 59
  year: 2010
  ident: B62
  article-title: High Expression Levels of Putative Hepatic Stem/Progenitor Cell Biomarkers Related to Tumour Angiogenesis and Poor Prognosis of Hepatocellular Carcinoma
  publication-title: Gut
  doi: 10.1136/gut.2008.176271
– volume: 9
  year: 2019
  ident: B30
  article-title: RACK1 Promotes Self-Renewal and Chemoresistance of Cancer Stem Cells in Human Hepatocellular Carcinoma Through Stabilizing Nanog
  publication-title: Theranostics
  doi: 10.7150/thno.29271
– volume: 141
  year: 2019
  ident: B32
  article-title: Nucleolin Is a Functional Binding Protein for Salinomycin in Neuroblastoma Stem Cells
  publication-title: J Am Chem Soc
  doi: 10.1021/jacs.8b12872
– volume: 72
  start-page: 100816
  year: 2020
  ident: B3
  article-title: Circulating Tumor Cell As the Functional Aspect of Liquid Biopsy to Understand the Metastatic Cascade in Solid Cancer
  publication-title: Mol Aspects Med
  doi: 10.1016/j.mam.2019.07.008
– volume: 9
  year: 2019
  ident: B20
  article-title: HBX-Induced miR-5188 Impairs FOXO1 to Stimulate β-Catenin Nuclear Translocation and Promotes Tumor Stemness in Hepatocellular Carcinoma
  publication-title: Theranostics
  doi: 10.7150/thno.37717
– volume: 10
  start-page: 99
  year: 2006
  ident: B53
  article-title: Prediction of Venous Metastases, Recurrence, and Prognosis in Hepatocellular Carcinoma Based on A Unique Immune Response Signature of the Liver Microenvironment
  publication-title: Cancer Cell
  doi: 10.1016/j.ccr.2006.06.016
– volume: 2
  year: 2012
  ident: B23
  article-title: Paracrine Signaling Between Carcinoma Cells and Mesenchymal Stem Cells Generates Cancer Stem Cell Niche Via Epithelial-Mesenchymal Transition
  publication-title: Cancer Discov
  doi: 10.1158/2159-8290.cd-12-0312
– volume: 158
  year: 2014
  ident: B4
  article-title: Circulating Tumor Cell Clusters Are Oligoclonal Precursors of Breast Cancer Metastasis
  publication-title: Cell
  doi: 10.1016/j.cell.2014.07.013
– volume: 12
  start-page: 59
  year: 2016
  ident: B48
  article-title: Chromosome Region Maintenance 1 Expression and Its Association With Clinical Pathological Features in Primary Carcinoma of the Liver
  publication-title: Exp Ther Med
  doi: 10.3892/etm.2016.3283
– volume: 36
  year: 2017
  ident: B44
  article-title: HOXB7 Accelerates the Malignant Progression of Hepatocellular Carcinoma by Promoting Stemness and Epithelial-Mesenchymal Transition
  publication-title: J Exp Clin Cancer Res
  doi: 10.1186/s13046-017-0559-4
– volume: 10
  year: 2020
  ident: B21
  article-title: Cancer Stem Cells and Epithelial-to-Mesenchymal Transition in Cancer Metastasis
  publication-title: Cold Spring Harb Perspect Med
  doi: 10.1101/cshperspect.a036905
– volume: 10
  year: 2018
  ident: B59
  article-title: Cancer Stem Cells in Hepatocellular Carcinoma: An Overview and Promising Therapeutic Strategies
  publication-title: Ther Adv Med Oncol
  doi: 10.1177/1758835918816287
– volume: 48
  year: 2015
  ident: B52
  article-title: Self-Renewal and Circulating Capacities of Metastatic Hepatocarcinoma Cells Required For Collaboration Between TM4SF5 and CD44
  publication-title: Bmb Rep
  doi: 10.5483/BMBRep.2015.48.3.047
– reference: 39050582 - Front Oncol. 2024 Jul 10;14:1438731. doi: 10.3389/fonc.2024.1438731
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Snippet Cancer stem cells (CSCs) and Circulating tumor cells (CTCs) have been proposed as fundamental causes for the recurrence of hepatocellular carcinoma (HCC). CTCs...
BackgroundCancer stem cells (CSCs) and Circulating tumor cells (CTCs) have been proposed as fundamental causes for the recurrence of hepatocellular carcinoma...
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SubjectTerms cancer stem cells
circulating tumor cells
epithelial-mesenchymal
hepatocellular carcinoma
Oncology
recurrence
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Title Association of Preoperative NANOG-Positive Circulating Tumor Cell Levels With Recurrence of Hepatocellular Carcinoma
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