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社论:染色体与人类肿瘤。运用新染色技术所取得的成果。

Editorial: Chromosomes and human neoplasms. Achievements using new staining techniques.

作者信息

Müller H, Stalder G R

出版信息

Eur J Pediatr. 1976 Aug 16;123(1):1-13. doi: 10.1007/BF00497675.

DOI:10.1007/BF00497675
PMID:60237
Abstract

Numerical and structural chromosome aberrations are frequently found in neoplastic cells. As demonstrated by the new chromosome banding techniques these aberrations are not random, but tend to show a specific occurrence. A model example is the leukemias where many cytogenetical investigations have been done to date. In leukemia chromosome analysis serves the following purposes: to identify a neoplastic process, to confirm and strengthen the hematological diagnosis, for the early diagnosis of transformation from a chronic leukemia into its blastic phase and for following up the clonal evolution of a leukemic cell line. In the discussion of chromosomes and neoplasms it must be mentioned that individuals demonstrating chromosomal instability and some trisomic patients show a greater tendency toward the development of a malignancy. Malignancy is primarily a cellular phenomenon caused by a disturbance in cellular regulation, whose fine events are not known. Therefore the exact role of the chromosomes in neoplastic processes cannot be stated. From experimental investigations it appears that the affected chromosomes carry cell growth regulating factors and also that a specific aberration is the result of the action of a specific agent.

摘要

在肿瘤细胞中经常发现染色体数目和结构异常。正如新的染色体显带技术所表明的,这些异常并非随机出现,而是倾向于呈现特定的发生情况。一个典型的例子是白血病,迄今为止已经进行了许多细胞遗传学研究。在白血病中,染色体分析有以下目的:识别肿瘤过程、确认并加强血液学诊断、早期诊断慢性白血病向原始细胞阶段的转化以及追踪白血病细胞系的克隆进化。在讨论染色体与肿瘤时,必须提到表现出染色体不稳定的个体以及一些三体患者有更大的患恶性肿瘤倾向。恶性肿瘤主要是一种由细胞调节紊乱引起的细胞现象,其具体机制尚不清楚。因此,无法确切说明染色体在肿瘤过程中的作用。从实验研究来看,受影响的染色体携带细胞生长调节因子,而且特定的异常是特定因素作用的结果。

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1
Editorial: Chromosomes and human neoplasms. Achievements using new staining techniques.社论:染色体与人类肿瘤。运用新染色技术所取得的成果。
Eur J Pediatr. 1976 Aug 16;123(1):1-13. doi: 10.1007/BF00497675.
2
Nonrandom chromosomal aberrations and clonal chromosomal evolution in acute leukemia associated with Down's syndrome.唐氏综合征相关急性白血病中的非随机染色体畸变与克隆性染色体进化
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Significance of chromosome abnormalities in leukemia.染色体异常在白血病中的意义。
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[Chromosomal abnormalities of the blastic phase of chronic myeloid leukemia].[慢性髓性白血病急变期的染色体异常]
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Chromosome abnormalities in human leukemia.人类白血病中的染色体异常
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引用本文的文献

1
[Chromosomal abnormalities in human neoplasia (author's transl)].人类肿瘤中的染色体异常(作者译)
Klin Wochenschr. 1978 Aug 1;56(15):733-41. doi: 10.1007/BF01476762.

本文引用的文献

1
Chromosome studies on normal and leukemic human leukocytes.对正常和白血病人类白细胞的染色体研究。
J Natl Cancer Inst. 1960 Jul;25:85-109.
2
Neoplasms in persons treated with x rays in infancy for thymic enlargement. A report of the third follow-up survey.婴儿期因胸腺肿大接受X射线治疗者的肿瘤。第三次随访调查报告。
J Natl Cancer Inst. 1967 Mar;38(3):317-41.
3
Cytogenetic observations in children with neuroblastoma.神经母细胞瘤患儿的细胞遗传学观察
Pediatrics. 1971 May;47(5):839-43.
4
Marrow chromosome studies in "preleukemia". Further correlation with clinical course.“白血病前期”的骨髓染色体研究。与临床病程的进一步相关性。
Cancer. 1971 Aug;28(2):513-8. doi: 10.1002/1097-0142(197108)28:2<513::aid-cncr2820280233>3.0.co;2-0.
5
Spontaneous chromosomal breakage and high incidence of leukemia in inherited disease.遗传性疾病中的自发染色体断裂和白血病高发病率。
Blood. 1971 Jan;37(1):96-112.
6
Suppression of malignancy by cell fusion.通过细胞融合抑制恶性肿瘤
Nature. 1969 Jul 26;223(5204):363-8. doi: 10.1038/223363a0.
7
Mutation and cancer: statistical study of retinoblastoma.突变与癌症:视网膜母细胞瘤的统计学研究
Proc Natl Acad Sci U S A. 1971 Apr;68(4):820-3. doi: 10.1073/pnas.68.4.820.
8
Oncogenes of RNA tumor viruses as determinants of cancer.作为癌症决定因素的RNA肿瘤病毒癌基因。
Proc Natl Acad Sci U S A. 1969 Nov;64(3):1087-94. doi: 10.1073/pnas.64.3.1087.
9
Clonal origin of chronic myelocytic leukemia in man.人类慢性粒细胞白血病的克隆起源。
Proc Natl Acad Sci U S A. 1967 Oct;58(4):1468-71. doi: 10.1073/pnas.58.4.1468.
10
The protovirus hypothesis: speculations on the significance of RNA-directed DNA synthesis for normal development and for carcinogenesis.原病毒假说:关于RNA指导的DNA合成在正常发育和致癌作用中的意义的推测。
J Natl Cancer Inst. 1971 Feb;46(2):3-7.