[1] Takahashi K, Yamanaka S. Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors[J]. Cell, 2006, 126:663-676. [2] Li Z, Rana TM. A kinase inhibitor screen identifies small-molecule enhancers of reprogramming and iPS cell generation[J]. Nature Communications, 2012, 3:1085. [3] Jiang J, Lv W, Ye X, et al. Zscan4 promotes genomic stability during reprogramming and dramatically improves the quality of iPS cells as demonstrated by tetraploid complementation[J]. Cell Res, 2013, 23(1):92-106. [4] Liang G, He J, Zhang Y. Kdm2b promotes induced pluripotent stem cell generation by facilitating gene activation early in reprogramming[J]. Nat Cell Biol, 2012, 14(5):457-466. [5] Chen J, Liu H, Liu J, et al. H3K9 methylation is a barrier during somatic cell reprogramming into iPSCs[J]. Nat Genet, 2012, 45:34-42. [6] Soufi A, Donahue G, Zaret KS. Facilitators and impediments of the pluripotency reprogramming factors’ initial engagement with the genome[J]. Cell, 2012, 151(5):994-1004. [7] Gore A, Li Z, Fung HL, et al. Somatic coding mutations in human induced pluripotent stem cells[J]. Nature, 2011, 471:63-67. [8] Mayshar Y, Ben-David U, Lavon N, et al. Identification and classification of chromosomal aberrations in human induced pluripotent stem cells[J]. Cell Stem Cell, 2010, 7:521-531. [9] Laurent LC, Ulitsky I, Slavin I, et al. Dynamic changes in the copy number of pluripotency and cell proliferation genes in human ESCs and iPSCs during reprogramming and time in culture[J]. Cell Stem Cell, 2011, 8:106-118. [10] Macheda ML, Rogers S, Best JD. Molecular and cellular regulation of glucose transporter(GLUT)proteins in cancer[J]. J Cell Physiol, 2005, 202(3):654-662. [11] Minina IM, Zhdanova NS, Shilov AG, et al. Chromosomal instability of in vitro cultured mouse embryonic stem cells and induced pluripotent stem cells[J]. Tsitologiia, 2010, 52:420-425. [12] Hussein SM, Batada NN, Vuoristo S, et al. Copy number variation and selection during reprogramming to pluripotency[J]. Nature, 2011, 471:58-62. [13] Lister R, Pelizzola M, Kida YS, et al. Hotspots of aberrant epigenomic reprogramming in human induced pluripotent stem cells[J]. Nature, 2011, 471:68-73. [14] Okita K, Ichisaka T, Yamanaka S. Generation of germline-competent induced pluripotent stem cells[J]. Nature, 2007, 448:313-317. [15] Nakagawa M, Koyanagi M, Tanabe K, et al. Generation of induced pluripotent stem cells without Myc from mouse and human fibroblasts[J]. Nat Biotechnol, 2008, 26:101-106. [16] Nagata S, Toyoda M, Yamaguchi S, et al. Efficient reprogramming of human and mouse primary extra-embryonic cells to pluripotent stem cells[J]. Genes Cells, 2009, 14:1395-1404. [17] Pasi CE, Dereli-Oz A, Negrini S, et al. Genomic instability in induced stem cells[J]. Cell Death Differ, 2011, 18:745-753. [18] Mills KD, Ferguson DO, Alt FW. The role of DNA breaks in genomic instability and tumorigenesis[J]. Immunol Rev, 2003, 194:77-95. [19] Ben-David U, Benvenisty N. The tumorigenicity of human embryonic and induced pluripotent stem cells[J]. Nature Reviews Cancer, 2011, 11:268-277. [20] Abyzov A, Mariani J, Palejev D, et al. Somatic copy number mosaicism in human skin revealed by induced pluripotent stem cells[J]. Nature, 2012, 492:438-442. [21] Hu J, Sun L, Shen F, et al. The intra-S phase checkpoint targets Dna2 to prevent stalled replication forks from reversing[J]. Cell, 2012, 149(6):1221-1232. [22] Hicks WM, Yamaguchi M, Haber JE. Real-time analysis of double-strand DNA break repair by homologous recombination[J]. PNAS, 2011, 108:3108-3115. [23] S? abicki M, Theis M, Krastev DB, et al. A genome-scale DNA repair RNAi screen identifies SPG48 as a novel gene associated with hereditary spastic paraplegia[J]. PLoS Biol, 2010, 8(6):e1000408. [24] Emre NC, Ingvarsdottir K, Wyce A, et al. Maintenance of low histone ubiquitylation by Ubp10 correlates with telomere-proximal Sir2 association and gene silencing[J]. Mol Cell, 2005, 17(4):585-594. [25] 陈忠民, 霍艳英, 吴德昌. PTEN在基因组稳定性中的作用[J]. 医学分子生物学杂志, 2008, 5(3):247-250. [26] Francia S, Michelini F, Saxena A, et al. Site-specific DICER and DROSHA RNA products control the DNA-damage response[J]. Nature, 2012, 488:231-235. [27] Murphy KL, Dennis AP, Rosen JM. A gain of function p53 mutant promotes both genomic instability and cell survival in a novel p53-null mammary epithelial cell model[J]. FASEB J, 2000, 14:2291-2302. [28] Ye D, Wang G, Liu Y, et al. MiR-138 promotes induced pluripotent stem cell generation through the regulation of the p53 signaling[J]. Stem Cells, 2012, 30(8):1645-1654. [29] Choi YJ, Lin CP, Ho JJ, et al. miR-34 miRNAs provide a barrier for somatic cell reprogramming[J]. Nat Cell Biol, 2011, 13(11):1353-1360. [30] Wang J, He Q, Han C, et al. p53-facilitated miR-199a-3p regulates somatic cell reprogramming[J]. Stem Cells, 2012, 30(7):1405-1413. [31] Hansson J, Rafiee MR, Reiland S, et al. Highly coordinated proteome dynamics during reprogramming of somatic cells to pluripotency[J]. Cell Reports, 2012, 2(6):1579-1592. [32] Takeichi M, Atsumi T, Yoshida C, et al. Selective adhesion of embryonal carcinoma cells and differentiated cells by Ca2+-dependent sites[J]. Dev Biol, 1981, 87:340-350. [33] Chen T, Yuan D, Wei B, et al. E-cadherin-mediated cell-cell contact is critical for induced pluripotent stem cell generation[J]. Stem Cells, 2010, 28(8):1315-1325. [34] Redmer T, Diecke S, Grigoryan T, et al. E-cadherin is crucial for embryonic stem cell pluripotency and can replace OCT4 during so-matic cell reprogramming[J]. EMBO Repo, 2011, 12:720-726. [35] Beddington RS, Robertson EJ. An assessment of the developmental potential of embryonic stem cells in the midgestation mouse embryo[J]. Development, 1989, 105:733-737. [36] Ohtsuka S, Nishikawa-Torikai S, Niwa H. E-cadherin promotes inc- orporation of mouse epiblast stem cells into normal development [J]. PLoS ONE, 2012, 7(9):e45220. [37] Li H, Collado M, Villasante A, et al. The Ink4/Arf locus is a barrier for iPS cell reprogramming[J]. Nature, 2009, 460:1136-1139. [38] Doege CA, Inoue K, Yamashita T, et al. Early-stage epigenetic modification during somatic cell reprogramming by Parp1 and Tet2[J]. Nature, 2012, 488:652-655. [39] Park IH, Arora N, Huo H, et al. Disease-specific induced pluripotent stem cells[J].Cell, 2008, 134(5):877-886. [40] Diekman BO, Christoforou N, Willard VP, et al. Cartilage tissue engineering using differentiated and purified induced pluripotent stem cells[J]. PNAS, 2012, 109(47):19172-19177. [41] Araki R, Uda M, Hoki Y, et al. Negligible immunogenicity of terminally differentiated cells derived from induced pluripotent or embryonic stem cells[J]. Nature, 2013, 494(7435):100-104. |