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Biomaterial-based platforms for cancer stem cell enrichment and study 被引量:3

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摘要 Cancer stem cells(CSCs)are a relatively rare subpopulation of tumor cell with self-renewal and tumorigenesis capabilities.CSCs are associated with cancer recurrence,progression,and chemoradiotherapy resistance.Establishing a reliable platform for CSC enrichment and study is a prerequisite for understanding the characteristics of CSCs and discovering CSC-related therapeutic strategies.Certain strategies for CSC enrichment have been used in laboratory,particularly fluorescence-activated cell sorting(FACS)and mammosphere culture.However,these methods fail to recapitulate the in vivo chemical and physical conditions in tumors,thus potentially decreasing the malignancy of CSCs in culture and yielding unreliable research results.Accumulating research suggests the promise of a biomaterial-based three-dimensional(3 D)strategy for CSC enrichment and study.This strategy has an advantage over conventional methods in simulating the tumor microenvironment,thus providing a more effective and predictive model for CSC laboratory research.In this review,we first briefly discuss the conventional methods for CSC enrichment and study.We then summarize the latest advances and challenges in biomaterial-based 3 D CSC platforms.Design strategies for materials,morphology,and chemical and physical cues are highlighted to provide direction for the future construction of platforms for CSC enrichment and study.
出处 《Cancer Biology & Medicine》 SCIE CAS CSCD 2021年第2期458-469,共12页 癌症生物学与医学(英文版)
基金 supported by grants from the National Natural Science Foundation of China(Grant Nos.11832008 and 81703012) the Program of the Postgraduate Tutor Team of Chongqing Education Commission(2018) the Fundamental Research Funds for the Central Universities(Grant No.2019CDXYSG0004) the Visiting Scholar Foundation of the Key Laboratory of Biorheological Science and Technology(Chongqing University),Ministry of Education(Grant No.CQKLBST-2017-005)。
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  • 1Ding S, Schultz PG. A role for chemistry in stem cell biology Nat Biotechnol 2004; 22: 833-840 [PMID: 15229546 DOI:10.1038/nbt987].
  • 2[K] Rao BM, Zandstra PW. Culture development for humanembryonic stem cell propagation: molecular aspects andchallenges. Curr Opin Biotechnol 2005; 16: 568-576 [PMID:16099157 DOI: 10.1016/j.copbio.2005.08.001].
  • 3[K]Moore KA, Lemischka IR. Stem cells and their niches. Science2006; 311: 1880-1885 [PMID: 16574858].
  • 4[K]Knoepfler PS. Deconstructing stem cell tumorigenicity: aroadmap to safe regenerative medicine. Stem Cells 2009; 27:1050-1056 [PMID: 19415771 DOI: 10.1002/stem.37].
  • 5[K]Pittenger MF, Mackay AM, Beck SC, Jaiswal RK, Douglas R,Mosca JD, Moorman MA, Simonetti DW, Craig S, MarshakDR. Multilineage potential of adult human mesenchymalstem cells. Science 1999; 284: 143-147 [PMID: 10102814 DOI:10.1126/science.284.5411.143].
  • 6[K] Puetzer JL, Petitte JN, Loboa EG. Comparative review ofgrowth factors for induction of three-dimensional in vitrochondrogenesis in human mesenchymal stem cells isolatedfrom bone marrow and adipose tissue. Tissue Eng part BRev 2010; 16: 435-44 [PMID: 20196646 DOI: 10.1089/ten.TEB.2009.0705].
  • 7[K] Mauney JR, Nguyen T, Gillen K, Kirker-Head C, GimbleJM, Kaplan DL. Engineering adipose-like tissue in vitro andin vivo utilizing human bone marrow and adipose-derivedmesenchymal stem cells with silk fibroin 3D scaffolds.Biomaterials 2007; 28: 5280-5290 [PMID: 17765303].
  • 8[K]Strau- S, Dudziak S, Hagemann R, Barcikowski S, Fliess M,Israelowitz M, Kracht D, Kuhbier JW, Radtke C, Reimers K,Vogt PM. Induction of osteogenic differentiation of adiposederived stem cells by microstructured nitinol actuatormediatedmechanical stress. PLoS One 2012; 7: e51264 [PMID:23236461 DOI: 10.1371/journal.pone.0051264].
  • 9[K]Even-Ram S, Artym V, Yamada KM. Matrix control of stemcell fate. Cell 2006; 126: 645-647 [PMID: 16923382].
  • 10[K] McNamara LE, McMurray RJ, Biggs MJ, Kantawong F,Oreffo RO, Dalby MJ. Nanotopographical control of stem celldifferentiation. J Tissue Eng 2010; 2010: 120623 [PMID: 21350640DOI: 10.4061/2010/120623].

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