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TS/A

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维基百科，自由的百科全书

TS/A是一種具有中等細胞分化能力的小鼠乳腺癌細胞系，最初在1983年分離自一隻二十個月大的雌性BALB/c小鼠的自發性腫瘤[1][2]。在1990年代，它被廣泛用作轉導細胞因子基因及其他具有免疫學意義的基因的受體細胞系，以生產誘導着抗腫瘤免疫反應的重組實驗疫苗[3]。因為具有異質性、低免疫原性及低轉移能力的特性而使其適合作為臨床前模型，並且可以應用於研究腫瘤-宿主相互作用和基因治療方法等。

特徵

TS/A細胞具有三倍體的核型[4]，並且在270位密碼子的位置帶有已突變的p53蛋白[5]，而大約三分之一的TS/A細胞均會表達癌症幹細胞標記物Sca-1（英语：Sca-1）[6]，有研究發現Sca-1的表達幾乎為陰性的TS/A細胞能被干擾素-γ誘導[7]，使其也能夠表達Sca-1。TS/A細胞表達雌激素受體（英语：Estrogen receptor）[1]和內源性鼠類p185-erbB2產物[8]。

科研方面

當最初進行測試時，TS/A細胞並未賦予抵抗第二次攻擊的保護[1]，故而顯示出較低的免疫原性，此結論日後在其他研究中均得到證實[9]。TS/A細胞表達內源性逆轉錄病毒的Gp70env產物，其AH1免疫優勢I類抗原決定了簇可以通過H-2Ld呈遞被細胞毒性T細胞所識別[10]，而Gp70env抗原在大腸癌細胞系CT26等鼠類細胞系均存在着。在TS/A細胞中觀察到Ld的下調[11]，原因可能是因為免疫編輯過程，逃避了宿主的免疫應答。TS/A細胞通過多種機制對宿主的免疫應答產生抑制作用，例如選擇性丟失T細胞和B細胞中的STAT5a/b表達[12]，並且產生轉化生長因子β1（英语：TGF beta 1）[13]、調節性T細胞的誘導[14]、對自然殺傷劑的抗性[15]，以及會產生破壞造血功能的集落刺激因子[16][17]，最終導致脾腫大及白細胞增多[18][19]。

當皮下注射到BALB/c小鼠體內時，TS/A細胞引起的局部腫瘤會迅速擴散到肺部。通過靜脈內途徑注射TS/A細胞後也可能觀察到轉移，因此可以比較轉移過程早期和晚期的動力學[1][20]。在培養過程可以觀察到TS/A細胞的異質性，因為它具有上皮樣和成纖維細胞樣形態，以及在培養物不依賴貼壁的生長方式[1][21]。從瓊脂培養物中，TS/A細胞可以分離出兩種類型的克隆細胞，既有致瘤性及轉移性，但轉移能力明顯不同[21]。與具低轉移性的成纖維細胞樣克隆細胞相比，高轉移性克隆出乎意料地普遍存在着。幾種鼠類乳腺癌細胞系的基因表達譜都顯示，TS/A-E1細胞（即高轉移性的克隆細胞）與高度表達封閉蛋白的簇聚在一起[22]。有基因表達譜數據表明，封閉蛋白-3是高轉移性克隆細胞中表達最高的基因，甚至比低轉移性克隆表達高約90倍，而低轉移性的克隆細胞則過度表達着NME4和神經細胞生長抑制因子等。

腫瘤-宿主相互作用

TS/A細胞誘導的腫瘤具有豐富且具異質性的浸潤物，包括粒細胞及單核細胞/巨噬細胞亞群（subpopulations），而它們的相對比例在腫瘤的進展過程中發生變化[23]。這與已知的髓樣細胞可塑性一致。幾個亞群通過多種機制，有助於在TS/A腫瘤中，維持着能夠促進腫瘤生長的微環境[24]。M2巨噬細胞是白細胞介素-10的大規模產生者，同時也是產生調節T細胞、輔助型T細胞、嗜酸性粒細胞和嗜鹼性球的幾種趨化因子的大規模產生者[24]。骨髓分離的抑制性細胞（英语：Myeloid-derived suppressor cell）（MDSC）是具異質性及未成熟的CD11b+/Gr-1+群體[25]，並且具有免疫抑制功能。目前已在TS/A模型系統中，研究了已極化的M2巨噬細胞及MDSC，以及規避促進腫瘤生長的策略，將已浸潤的細胞轉變為細胞分化程度更高的細胞。在TS/A模型中，M2腫瘤巨噬細胞的誘導是由CD20同源MS4A8A基因的表達所介導[26]。在TS/A腫瘤中，處於低氧性腫瘤區域的極化M2巨噬細胞數量更為豐富[23]，並且促進血管的生成。在TS/A腫瘤中，交替激活的M2腫瘤相關巨噬細胞表達着STAB1（英语：STAB1），其參與着將有害成分的吞噬過程，已經發現STAB1包含着細胞外基質骨結合素（英语：Osteonectin）（一種腫瘤抑制劑）的可溶成分。有研究指出Stabilin-1可能通過提高SPARC的清除率，從而在TS/A模型中發揮着促進腫瘤生長的作用[27]。

在TS/A腫瘤微環境中，其他非腫瘤細胞類型也可以起到促進腫瘤生長的作用，例如與腫瘤相關的成纖維細胞和脂肪細胞。通過腫瘤基質細胞共注射模型，在腫瘤相關的成纖維細胞中鑑定出新的候選腫瘤相關基因。微管蛋白酪氨酸連接酶（英语：Tubulin—tyrosine ligase）是研究最多的基因，其在腫瘤相關成纖維細胞中的表達下調，促進了TS/A腫瘤的生長[28]。TS/A細胞與脂肪細胞一起培養的話，將導致TS/A細胞中脂質含量的增加，以及肺部定植能力的提高[29]。從脂滴釋放的游離脂肪酸是由三酸甘油脂水解酶（英语：Adipose triglyceride lipase）依賴性的脂解途徑所介導的，而該途徑則被認為是潛在的治療靶標。腫瘤細胞與腫瘤相關脂肪細胞之間的代謝串擾，可能有利於上皮-間質轉化（epithelial-mesenchymal transition），並且增加腫瘤的侵襲性。

TS/A細胞像其他腫瘤細胞系般分泌着外排體，然而在腫瘤生物學中起著相反的作用。外排體可能具有一定的免疫刺激作用。因為它們攜帶的腫瘤抗原可以轉移到樹突狀細胞及細胞毒性T細胞[30]。然而外排體主要通過抑制着自然殺傷細胞的功能[31]及抑制骨髓樹突狀細胞進行分化[32]，從而發揮有效的免疫抑制性抗腫瘤免疫反應。經照射的TS/A細胞所釋出的外排體顯示出分子組成的改變，並且能夠將雙鏈DNA（dsDNA）轉移到樹突狀細胞中，並且令共激分子（co-stimulatory molecules）的表達上調，以及引起STING（英语：Stimulator of interferon genes）依賴性的干擾素-1（英语：Interferon type I）激活[33]。

參考資料

  1. ^ 1.0 1.1 1.2 1.3 1.4 Nanni, P; de Giovanni, C; Lollini, PL; Nicoletti, G; Prodi, G. TS/A: a new metastasizing cell line from a BALB/c spontaneous mammary adenocarcinoma.. Clinical & experimental metastasis. NaN, 1 (4): 373–80 [2020-01-10]. PMID 6546207. doi:10.1007/bf00121199.  [永久失效連結]
  2. ^ De Giovanni, C; Nicoletti, G; Landuzzi, L; Palladini, A; Lollini, PL; Nanni, P. Bioprofiling TS/A Murine Mammary Cancer for a Functional Precision Experimental Model.. Cancers. 2019-11-27, 11 (12) [2020-01-10]. PMID 31783695. doi:10.3390/cancers11121889. [永久失效連結]
  3. ^ Allione, A; Consalvo, M; Nanni, P; Lollini, PL; Cavallo, F; Giovarelli, M; Forni, M; Gulino, A; Colombo, MP; Dellabona, P. Immunizing and curative potential of replicating and nonreplicating murine mammary adenocarcinoma cells engineered with interleukin (IL)-2, IL-4, IL-6, IL-7, IL-10, tumor necrosis factor alpha, granulocyte-macrophage colony-stimulating factor, and gamma-interferon gene or admixed with conventional adjuvants.. Cancer research. 1994-12-01, 54 (23): 6022–6 [2020-01-10]. PMID 7954438. [永久失效連結]
  4. ^ Jentsch, I; Geigl, J; Klein, CA; Speicher, MR. Seven-fluorochrome mouse M-FISH for high-resolution analysis of interchromosomal rearrangements.. Cytogenetic and genome research. 2003, 103 (1-2): 84–8 [2020-01-10]. PMID 15004469. doi:10.1159/000076294. [永久失效連結]
  5. ^ Odin, L; Favrot, M; Poujol, D; Michot, JP; Moingeon, P; Tartaglia, J; Puisieux, I. Canarypox virus expressing wild type p53 for gene therapy in murine tumors mutated in p53.. Cancer gene therapy. 2001-02, 8 (2): 87–98 [2020-01-10]. PMID 11263530. doi:10.1038/sj.cgt.7700279. [永久失效連結]
  6. ^ Kim, RJ; Kim, SR; Roh, KJ; Park, SB; Park, JR; Kang, KS; Kong, G; Tang, B; Yang, YA; Kohn, EA; Wakefield, LM; Nam, JS. Ras activation contributes to the maintenance and expansion of Sca-1pos cells in a mouse model of breast cancer.. Cancer letters. 2010-01-28, 287 (2): 172–81 [2020-01-10]. PMID 19586713. doi:10.1016/j.canlet.2009.06.010. [永久失效連結]
  7. ^ Lollini, PL; Bosco, MC; Cavallo, F; De Giovanni, C; Giovarelli, M; Landuzzi, L; Musiani, P; Modesti, A; Nicoletti, G; Palmieri, G. Inhibition of tumor growth and enhancement of metastasis after transfection of the gamma-interferon gene.. International journal of cancer. 1993-09-09, 55 (2): 320–9 [2020-01-10]. PMID 8370628. doi:10.1002/ijc.2910550224. [永久失效連結]
  8. ^ Hsu, HC; Li, L; Zhang, HG; Mountz, JD. Genetic regulation of thymic involution.. Mechanisms of ageing and development. 2005-01, 126 (1): 87–97 [2020-01-10]. PMID 15610766. doi:10.1016/j.mad.2004.09.016. [永久失效連結]
  9. ^ Cavallo, F; Giovarelli, M; Gulino, A; Vacca, A; Stoppacciaro, A; Modesti, A; Forni, G. Role of neutrophils and CD4+ T lymphocytes in the primary and memory response to nonimmunogenic murine mammary adenocarcinoma made immunogenic by IL-2 gene.. Journal of immunology (Baltimore, Md. : 1950). 1992-12-01, 149 (11): 3627–35 [2020-01-10]. PMID 1358974. [永久失效連結]
  10. ^ Rosato, A; Dalla Santa, S; Zoso, A; Giacomelli, S; Milan, G; Macino, B; Tosello, V; Dellabona, P; Lollini, PL; De Giovanni, C; Zanovello, P. The cytotoxic T-lymphocyte response against a poorly immunogenic mammary adenocarcinoma is focused on a single immunodominant class I epitope derived from the gp70 Env product of an endogenous retrovirus.. Cancer research. 2003-05-01, 63 (9): 2158–63 [2020-01-10]. PMID 12727834. [永久失效連結]
  11. ^ Schirmbeck, R; Riedl, P; Kupferschmitt, M; Wegenka, U; Hauser, H; Rice, J; Kröger, A; Reimann, J. Priming protective CD8 T cell immunity by DNA vaccines encoding chimeric, stress protein-capturing tumor-associated antigen.. Journal of immunology (Baltimore, Md. : 1950). 2006-08-01, 177 (3): 1534–42 [2020-01-10]. PMID 16849460. doi:10.4049/jimmunol.177.3.1534. [永久失效連結]
  12. ^ Pericle, F; Kirken, RA; Bronte, V; Sconocchia, G; DaSilva, L; Segal, DM. Immunocompromised tumor-bearing mice show a selective loss of STAT5a/b expression in T and B lymphocytes.. Journal of immunology (Baltimore, Md. : 1950). 1997-09-15, 159 (6): 2580–5 [2020-01-10]. PMID 9300676. [永久失效連結]
  13. ^ Kummar, S; Ishii, A; Yang, HK; Venzon, DJ; Kim, SJ; Gress, RE. Modulation of graft-versus-tumor effects in a murine allogeneic bone marrow transplantation model by tumor-derived transforming growth factor-betaI.. Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation. 2001, 7 (1): 25–30 [2020-01-10]. PMID 11215695. doi:10.1053/bbmt.2001.v7.pm11215695. [永久失效連結]
  14. ^ Piconese, S; Valzasina, B; Colombo, MP. OX40 triggering blocks suppression by regulatory T cells and facilitates tumor rejection.. The Journal of experimental medicine. 2008-04-14, 205 (4): 825–39 [2020-01-10]. PMID 18362171. doi:10.1084/jem.20071341. [永久失效連結]
  15. ^ Morandi, B; Mortara, L; Chiossone, L; Accolla, RS; Mingari, MC; Moretta, L; Moretta, A; Ferlazzo, G. Dendritic cell editing by activated natural killer cells results in a more protective cancer-specific immune response.. PloS one. 2012, 7 (6): e39170 [2020-01-10]. PMID 22723958. doi:10.1371/journal.pone.0039170. [永久失效連結]
  16. ^ Nicoletti, G; Brambilla, P; De Giovanni, C; Lollini, PL; Del Re, B; Marocchi, A; Mocarelli, P; Prodi, G; Nanni, P. Colony-stimulating activity from the new metastatic TS/A cell line and its high- and low-metastatic clonal derivatives.. British journal of cancer. 1985-08, 52 (2): 215–22 [2020-01-10]. PMID 3875361. doi:10.1038/bjc.1985.180. [永久失效連結]
  17. ^ Nicoletti, G; Lollini, PL; Bagnara, GP; De Giovanni, C; Del Re, B; Bons, L; Prodi, G; Nanni, P. Are colony-stimulating factor-producing cells facilitated in the metastatic process?. Anticancer research. NaN, 7 (4B): 695–700 [2020-01-10]. PMID 3314670.  [永久失效連結]
  18. ^ Bronte, V; Apolloni, E; Cabrelle, A; Ronca, R; Serafini, P; Zamboni, P; Restifo, NP; Zanovello, P. Identification of a CD11b(+)/Gr-1(+)/CD31(+) myeloid progenitor capable of activating or suppressing CD8(+) T cells.. Blood. 2000-12-01, 96 (12): 3838–46 [2020-01-10]. PMID 11090068. [永久失效連結]
  19. ^ Sinha, P; Chornoguz, O; Clements, VK; Artemenko, KA; Zubarev, RA; Ostrand-Rosenberg, S. Myeloid-derived suppressor cells express the death receptor Fas and apoptose in response to T cell-expressed FasL.. Blood. 2011-05-19, 117 (20): 5381–90 [2020-01-10]. PMID 21450901. doi:10.1182/blood-2010-11-321752. [永久失效連結]
  20. ^ Nanni, P; De Giovanni, C; Lollini, PL; Nicoletti, G; Prodi, G. Clones with different metastatic capacity and variant selection during metastasis: a problematic relationship.. Journal of the National Cancer Institute. 1986-01, 76 (1): 87–93 [2020-01-10]. PMID 3455746. [永久失效連結]
  21. ^ 21.0 21.1 Lollini, PL; de Giovanni, C; Eusebi, V; Nicoletti, G; Prodi, G; Nanni, P. High-metastatic clones selected in vitro from a recent spontaneous BALB/c mammary adenocarcinoma cell line.. Clinical & experimental metastasis. NaN, 2 (3): 251–9 [2020-01-10]. PMID 6543703. doi:10.1007/bf00132932.  [永久失效連結]
  22. ^ Yang, Y; Yang, HH; Hu, Y; Watson, PH; Liu, H; Geiger, TR; Anver, MR; Haines, DC; Martin, P; Green, JE; Lee, MP; Hunter, KW; Wakefield, LM. Immunocompetent mouse allograft models for development of therapies to target breast cancer metastasis.. Oncotarget. 2017-05-09, 8 (19): 30621–30643 [2020-01-10]. PMID 28430642. doi:10.18632/oncotarget.15695. （原始内容存档于2019-12-27）. 
  23. ^ 23.0 23.1 Movahedi, K; Laoui, D; Gysemans, C; Baeten, M; Stangé, G; Van den Bossche, J; Mack, M; Pipeleers, D; In't Veld, P; De Baetselier, P; Van Ginderachter, JA. Different tumor microenvironments contain functionally distinct subsets of macrophages derived from Ly6C(high) monocytes.. Cancer research. 2010-07-15, 70 (14): 5728–39 [2020-01-11]. PMID 20570887. doi:10.1158/0008-5472.CAN-09-4672. （原始内容存档于2020-01-11）. 
  24. ^ 24.0 24.1 Galdiero, MR; Bonavita, E; Barajon, I; Garlanda, C; Mantovani, A; Jaillon, S. Tumor associated macrophages and neutrophils in cancer.. Immunobiology. 2013-11, 218 (11): 1402–10 [2020-01-11]. PMID 23891329. doi:10.1016/j.imbio.2013.06.003. （原始内容存档于2020-01-11）. 
  25. ^ Bronte, V; Brandau, S; Chen, SH; Colombo, MP; Frey, AB; Greten, TF; Mandruzzato, S; Murray, PJ; Ochoa, A; Ostrand-Rosenberg, S; Rodriguez, PC; Sica, A; Umansky, V; Vonderheide, RH; Gabrilovich, DI. Recommendations for myeloid-derived suppressor cell nomenclature and characterization standards.. Nature communications. 2016-07-06, 7: 12150 [2020-01-11]. PMID 27381735. doi:10.1038/ncomms12150. （原始内容存档于2020-01-11）. 
  26. ^ Schmieder, A; Schledzewski, K; Michel, J; Tuckermann, JP; Tome, L; Sticht, C; Gkaniatsou, C; Nicolay, JP; Demory, A; Faulhaber, J; Kzhyshkowska, J; Géraud, C; Goerdt, S. Synergistic activation by p38MAPK and glucocorticoid signaling mediates induction of M2-like tumor-associated macrophages expressing the novel CD20 homolog MS4A8A.. International journal of cancer. 2011-07-01, 129 (1): 122–32 [2020-01-11]. PMID 20824698. doi:10.1002/ijc.25657. （原始内容存档于2020-01-11）. 
  27. ^ Riabov, V; Yin, S; Song, B; Avdic, A; Schledzewski, K; Ovsiy, I; Gratchev, A; Llopis Verdiell, M; Sticht, C; Schmuttermaier, C; Schönhaber, H; Weiss, C; Fields, AP; Simon-Keller, K; Pfister, F; Berlit, S; Marx, A; Arnold, B; Goerdt, S; Kzhyshkowska, J. Stabilin-1 is expressed in human breast cancer and supports tumor growth in mammary adenocarcinoma mouse model.. Oncotarget. 2016-05-24, 7 (21): 31097–110 [2020-01-11]. PMID 27105498. doi:10.18632/oncotarget.8857. 
  28. ^ Rong, L; Bian, Y; Liu, S; Liu, X; Li, X; Liu, H; Zhou, J; Peng, J; Zhang, H; Chen, H; Qin, Z. Identifying tumor promoting genomic alterations in tumor-associated fibroblasts via retrovirus-insertional mutagenesis.. Oncotarget. 2017-11-14, 8 (57): 97231–97245 [2020-01-11]. PMID 29228606. doi:10.18632/oncotarget.21881. 
  29. ^ Wang, YY; Attané, C; Milhas, D; Dirat, B; Dauvillier, S; Guerard, A; Gilhodes, J; Lazar, I; Alet, N; Laurent, V; Le Gonidec, S; Biard, D; Hervé, C; Bost, F; Ren, GS; Bono, F; Escourrou, G; Prentki, M; Nieto, L; Valet, P; Muller, C. Mammary adipocytes stimulate breast cancer invasion through metabolic remodeling of tumor cells.. JCI insight. 2017-02-23, 2 (4): e87489 [2020-01-11]. PMID 28239646. doi:10.1172/jci.insight.87489. 
  30. ^ Wolfers, J; Lozier, A; Raposo, G; Regnault, A; Théry, C; Masurier, C; Flament, C; Pouzieux, S; Faure, F; Tursz, T; Angevin, E; Amigorena, S; Zitvogel, L. Tumor-derived exosomes are a source of shared tumor rejection antigens for CTL cross-priming.. Nature medicine. 2001-03, 7 (3): 297–303 [2020-01-11]. PMID 11231627. doi:10.1038/85438. （原始内容存档于2020-01-11）. 
  31. ^ Liu, C; Yu, S; Zinn, K; Wang, J; Zhang, L; Jia, Y; Kappes, JC; Barnes, S; Kimberly, RP; Grizzle, WE; Zhang, HG. Murine mammary carcinoma exosomes promote tumor growth by suppression of NK cell function.. Journal of immunology (Baltimore, Md. : 1950). 2006-02-01, 176 (3): 1375–85 [2020-01-11]. PMID 16424164. doi:10.4049/jimmunol.176.3.1375. （原始内容存档于2020-01-11）. 
  32. ^ Yu, S; Liu, C; Su, K; Wang, J; Liu, Y; Zhang, L; Li, C; Cong, Y; Kimberly, R; Grizzle, WE; Falkson, C; Zhang, HG. Tumor exosomes inhibit differentiation of bone marrow dendritic cells.. Journal of immunology (Baltimore, Md. : 1950). 2007-06-01, 178 (11): 6867–75 [2020-01-11]. PMID 17513735. doi:10.4049/jimmunol.178.11.6867. （原始内容存档于2020-01-11）. 
  33. ^ Diamond, JM; Vanpouille-Box, C; Spada, S; Rudqvist, NP; Chapman, JR; Ueberheide, BM; Pilones, KA; Sarfraz, Y; Formenti, SC; Demaria, S. Exosomes Shuttle TREX1-Sensitive IFN-Stimulatory dsDNA from Irradiated Cancer Cells to DCs.. Cancer immunology research. 2018-08, 6 (8): 910–920 [2020-01-11]. PMID 29907693. doi:10.1158/2326-6066.CIR-17-0581. （原始内容存档于2020-01-11）. 

外部連結

检索自“https://zh.wikipedia.org/w/index.php?title=TS/A&oldid=74199896”