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为什么细胞毒性化疗只能治愈某些癌症?

Why does cytotoxic chemotherapy cure only some cancers?

作者信息

Savage Philip, Stebbing Justin, Bower Mark, Crook Tim

机构信息

Department of Medical Oncology, Imperial College School of Medicine, Charing Cross Hospital, Fulham Palace Road, London, UK.

出版信息

Nat Clin Pract Oncol. 2009 Jan;6(1):43-52. doi: 10.1038/ncponc1260. Epub 2008 Nov 4.

DOI:10.1038/ncponc1260
PMID:18982000
Abstract

Despite frequent responses to chemotherapy, curative treatment remains elusive for the majority of patients with metastatic solid tumors. By contrast, in testicular cancer, gestational choriocarcinoma, Hodgkin disease and high-grade lymphomas, chemotherapy is routinely curative, even for patients who present with widely disseminated disease. In the common advanced cancers, however, over 40 years of cytotoxic drug development has brought no significant change in cure rates. One interpretation is that the intrinsic properties of the malignancies themselves, rather than the qualities of individual drugs or combination therapies, are primarily responsible for their curability with chemotherapy. We suggest that the curability of these malignancies results from an intrinsic 'locked-in' state of sensitivity to proapoptotic stresses in these cells. A common property of such curable malignancies is that they arise from cells that undergo major genetic rearrangements or recombination as part of their normal physiology. The absence of further genetic and epigenetic changes in genes that regulate apoptosis, DNA repair and senescence allows these cells to maintain their intrinsic sensitivity to chemotherapy. This process allows the cells, when challenged with chemotherapy, to undergo the natural apoptotic pathways that contribute to their intrinsic qualities of chemosensitivity and high curability.

摘要

尽管大多数转移性实体瘤患者对化疗常有反应,但根治性治疗对他们中的大多数人来说仍然难以实现。相比之下,在睾丸癌、妊娠性绒毛膜癌、霍奇金病和高级别淋巴瘤中,化疗通常是根治性的,即使是对那些出现广泛播散性疾病的患者也是如此。然而,在常见的晚期癌症中,40多年的细胞毒性药物研发并未使治愈率有显著改变。一种解释是,恶性肿瘤本身的内在特性,而非个别药物或联合疗法的特性,是其化疗可治愈性的主要原因。我们认为,这些恶性肿瘤的可治愈性源于这些细胞对促凋亡应激的内在“锁定”敏感性状态。这类可治愈恶性肿瘤的一个共同特性是,它们起源于在正常生理过程中经历重大基因重排或重组的细胞。调节细胞凋亡、DNA修复和衰老的基因中不存在进一步的基因和表观遗传变化,使得这些细胞能够维持其对化疗的内在敏感性。这一过程使细胞在受到化疗挑战时,能够经历自然凋亡途径,这些途径促成了它们化疗敏感性和高治愈率的内在特性。

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Curr Opin Oncol. 2007 Sep;19(5):486-91. doi: 10.1097/CCO.0b013e3282dc94e5.
2
Heterogeneity of protein kinase C beta(2) expression in lymphoid malignancies.蛋白激酶Cβ(2)在淋巴系统恶性肿瘤中的表达异质性
Histopathology. 2007 Apr;50(5):561-6. doi: 10.1111/j.1365-2559.2007.02666.x.
3
Recent experience with decitabine in MDS.地西他滨治疗骨髓增生异常综合征的近期经验。
应对遗传性肿瘤异质性、治疗后转移扩散、癌症再增殖以及获得性肿瘤细胞耐药性的发展。
Cancers (Basel). 2023 Dec 29;16(1):180. doi: 10.3390/cancers16010180.
4
p‑STAT3 influences doxorubicin and etoposide resistance of A549 cells grown in an 3D culture model.p-STAT3 影响在 3D 培养模型中生长的 A549 细胞对多柔比星和依托泊苷的耐药性。
Oncol Rep. 2023 Apr;49(4). doi: 10.3892/or.2023.8508. Epub 2023 Feb 24.
5
Valid-NEO: A Multi-Omics Platform for Neoantigen Detection and Quantification from Limited Clinical Samples.Valid-NEO:一个用于从有限临床样本中检测和定量新抗原的多组学平台。
Cancers (Basel). 2022 Feb 28;14(5):1243. doi: 10.3390/cancers14051243.
6
Polygodial and Ophiobolin A Analogues for Covalent Crosslinking of Anticancer Targets.多穗柯因和蛇孢菌素 A 类似物用于抗癌靶点的共价交联。
Int J Mol Sci. 2021 Oct 19;22(20):11256. doi: 10.3390/ijms222011256.
7
Angiogenesis and chemotherapy resistance: optimizing chemotherapy scheduling using mathematical modeling.血管生成与化疗耐药:利用数学建模优化化疗方案。
J Cancer Res Clin Oncol. 2021 Aug;147(8):2281-2299. doi: 10.1007/s00432-021-03657-9. Epub 2021 May 29.
8
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9
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10
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BMC Med Genomics. 2019 Jun 17;12(1):87. doi: 10.1186/s12920-019-0519-2.
Clin Adv Hematol Oncol. 2007 Feb;5(2):140.
4
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J Biol Chem. 2007 Apr 27;282(17):13059-72. doi: 10.1074/jbc.M609038200. Epub 2007 Feb 28.
5
Impaired V(D)J recombination and increased apoptosis among B cell precursors in the bone marrow of c-Abl-deficient mice.c-Abl基因缺陷小鼠骨髓中B细胞前体的V(D)J重组受损及凋亡增加。
Int Immunol. 2007 Mar;19(3):267-76. doi: 10.1093/intimm/dxl143. Epub 2007 Jan 17.
6
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8
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10
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Nat Rev Immunol. 2006 Aug;6(8):573-83. doi: 10.1038/nri1896.