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相似文献

1
Chemically induced leukemia in humans.化学物质诱发的人类白血病。
Environ Health Perspect. 1981 Jun;39:93-103. doi: 10.1289/ehp.813993.
2
Radiation and drug therapies, and leukemia.放射疗法、药物疗法与白血病。
Annu Rev Med. 1973;24:75-82. doi: 10.1146/annurev.me.24.020173.000451.
3
Leukemia following chemotherapy for ovarian cancer.卵巢癌化疗后发生的白血病。
N Engl J Med. 1990 Jan 4;322(1):1-6. doi: 10.1056/NEJM199001043220101.
4
Chemical leukemogenesis in man.人类化学性白血病发生
Ser Haematol. 1974;7(2):211-23.
5
Acute leukemia after alkylating-agent therapy of ovarian cancer.卵巢癌经烷化剂治疗后发生的急性白血病。
N Engl J Med. 1977 Jul 28;297(4):177-81. doi: 10.1056/NEJM197707282970402.
6
Bone marrow depression induced by chloramphenicol or phenylbutazone. Leukemia and other sequelae.氯霉素或保泰松引起的骨髓抑制。白血病及其他后遗症。
JAMA. 1967 Sep 11;201(11):828-34.
7
Characteristics of secondary acute nonlymphocytic leukemias. Cytological aspects (a review).继发性急性非淋巴细胞白血病的特征。细胞学方面(综述)
Folia Haematol Int Mag Klin Morphol Blutforsch. 1984;111(2):180-5.
8
[The state of hemopoiesis in the regional perfusion of malignant tumors of the extremities with sarcolysin, thio-TEPA and cyclophosphane].[用溶肉瘤素、噻替派和环磷酰胺对四肢恶性肿瘤进行区域灌注时的造血状态]
Vopr Onkol. 1967;13(2):48-54.
9
Carcinogenic potency of alkylating agents in rodents and humans.烷化剂在啮齿动物和人类中的致癌效力。
Cancer Res. 1992 May 1;52(9):2464-7.
10
[Side-effects of cytostatic and immunosuppressive therapy].[细胞毒性和免疫抑制疗法的副作用]
Fortschr Med. 1973 Mar 22;91(9):357-62.

引用本文的文献

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Association between metal(loid)s in serum and leukemia: a systematic review and meta-analysis.血清中金属(类金属)与白血病之间的关联:一项系统评价和荟萃分析。
J Environ Health Sci Eng. 2023 Feb 13;21(1):201-213. doi: 10.1007/s40201-023-00853-2. eCollection 2023 Jun.
2
Combining QSAR Modeling and Text-Mining Techniques to Link Chemical Structures and Carcinogenic Modes of Action.结合定量构效关系建模与文本挖掘技术以关联化学结构与致癌作用模式
Front Pharmacol. 2016 Aug 30;7:284. doi: 10.3389/fphar.2016.00284. eCollection 2016.
3
Modeling marrow damage from response data: evolution from radiation biology to benzene toxicity.从反应数据建模骨髓损伤:从放射生物学到苯毒性的演变
Environ Health Perspect. 1996 Dec;104 Suppl 6(Suppl 6):1293-301. doi: 10.1289/ehp.961041293.
4
Cancer mortality among workers in the meat department of supermarkets.超市肉类部门员工的癌症死亡率。
Occup Environ Med. 1994 Aug;51(8):541-7. doi: 10.1136/oem.51.8.541.
5
Effects of DDT on the calcium transport and thymidine uptake of bovine lymphocytes.滴滴涕对牛淋巴细胞钙转运和胸苷摄取的影响。
Bull Environ Contam Toxicol. 1986 Oct;37(4):523-30. doi: 10.1007/BF01607799.
6
Occurrence of cancer in women in the meat industry.肉类行业女性患癌情况。
Br J Ind Med. 1986 Sep;43(9):597-604. doi: 10.1136/oem.43.9.597.

本文引用的文献

1
Phenylbutazone and Leukaemia.保泰松与白血病
Br Med J. 1960 Nov 26;2(5212):1552-5. doi: 10.1136/bmj.2.5212.1552.
2
CARCINOGENIC ACTIVITY OF A NEW ANTITUMOR AGENT, N-ISOPROPYL-ALPHA-(2-METHYLHYDRAZINO)-P-TOLUAMIDE, HYDROCHLORIDE (NSC-77213).一种新型抗肿瘤药物盐酸N-异丙基-α-(2-甲基肼基)-对甲苯酰胺(NSC-77213)的致癌活性
Cancer Chemother Rep. 1964 Jul;39:77-80.
3
LEUKAEMIA AND PHENYLBUTAZONE.白血病与保泰松
Br Med J. 1964 Oct 3;2(5413):875. doi: 10.1136/bmj.2.5413.875-c.
4
BENZENE AND LEUKEMIA.苯与白血病
N Engl J Med. 1964 Oct 22;271:872-6. doi: 10.1056/NEJM196410222711703.
5
LEUKAEMIA AND PHENYLBUTAZONE.白血病与保泰松
Br Med J. 1964 Aug 29;2(5408):569. doi: 10.1136/bmj.2.5408.569-a.
6
PHENYLBUTAZONE THERAPY ASSOCIATED WITH LEUKAEMIA.与白血病相关的保泰松治疗
Br Med J. 1964 Mar 21;1(5385):747. doi: 10.1136/bmj.1.5385.747.
7
ACUTE LEUKAEMIA ASSOCIATED WITH PHENYLBUTAZONE TREATMENT.与保泰松治疗相关的急性白血病
Br Med J. 1964 Mar 21;1(5385):744-6. doi: 10.1136/bmj.1.5385.744.
8
[Induction of a transplantable tumor in mice of a Swiss strain by repeated injections of chloramphenicol].[通过反复注射氯霉素在瑞士品系小鼠中诱导可移植性肿瘤]
Ann Pharm Fr. 1962 Feb;20:116-20.
9
Chloramphenicol bone marrowtoxicity.氯霉素骨髓毒性。
JAMA. 1961 May 20;176:588-93. doi: 10.1001/jama.1961.03040200024007.
10
Leukaemia following radioiodine treatment of thyrotoxicosis.甲状腺毒症放射性碘治疗后发生的白血病。
Br Med J. 1960 Nov 26;2(5212):1545-50. doi: 10.1136/bmj.2.5212.1545.

化学物质诱发的人类白血病。

Chemically induced leukemia in humans.

作者信息

Adamson R H, Seiber S M

出版信息

Environ Health Perspect. 1981 Jun;39:93-103. doi: 10.1289/ehp.813993.

DOI:10.1289/ehp.813993
PMID:6786872
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1568737/
Abstract

The human population may be exposed to potentially leukemogenic agents, either in the form of drugs and food additives or as environmental contaminants and pollutants. However, in spite of the large number and diversity of these chemicals, only a few have been implicated as human leukemogens. One such agent is benzene, a known bone marrow depressant. A number of case reports have associated chronic exposure to this agent with the development of acute leukemia, as have several epidemiologic surveys. Treatment with various antitumor agents, including procarbazine, melphalan, thio-TEPA, chlorambucil, and cyclophosphamide, has also been associated with the development of acute leukemia. In addition, chloramphenicol and phenylbutazone have been implicated as human leukemogens, but the association between exposure to these two agents and acute leukemia appears at present to be weaker than it is for benzene and antitumor agent exposure. Despite such associations between exposure to chemicals and acute leukemia, several important problems exist with regard to implicating specific agents in the development of this neoplasm in man, including the paucity of animal models for chemically induced leukemia, and the frequent necessity to rely on single case reports or clusters of cases in which chemical exposures are associated with acute leukemia. Future efforts should be directed at performing properly designed and well executed epidemiologic studies, and at developing new in vitro and in vivo models for the study of this neoplasm.

摘要

人类可能会接触到潜在的致白血病物质,这些物质可以是药物、食品添加剂的形式,也可以是环境污染物和污染物的形式。然而,尽管这些化学物质数量众多且种类各异,但只有少数几种被认为是人类白血病致癌物。其中一种物质是苯,一种已知的骨髓抑制剂。一些病例报告将长期接触这种物质与急性白血病的发生联系起来,一些流行病学调查也是如此。使用包括丙卡巴肼、美法仑、硫替派、苯丁酸氮芥和环磷酰胺在内的各种抗肿瘤药物进行治疗,也与急性白血病的发生有关。此外,氯霉素和保泰松也被认为是人类白血病致癌物,但目前看来,接触这两种物质与急性白血病之间的关联比接触苯和抗肿瘤药物的关联要弱。尽管接触化学物质与急性白血病之间存在这样的关联,但在确定特定物质与人类这种肿瘤发生之间的关系方面存在几个重要问题,包括化学诱导白血病的动物模型匮乏,以及经常需要依赖化学物质接触与急性白血病相关的单个病例报告或病例群。未来的努力应致力于开展设计合理、执行良好的流行病学研究,以及开发用于研究这种肿瘤的新的体外和体内模型。