Literature DB >> 15489132

Multistep and multifactorial carcinogenesis: when does a contributing factor become a carcinogen?

Michele Carbone1, Harvey I Pass.   

Abstract

Our greatest successes in fighting cancer derive from the identification and removal or inactivation of carcinogenic substances, and from the identification and removal of pre-malignant lesions. In comparison, our successes at treating already formed malignancies have been minimal. Therefore, emphasis should be put in identifying and removing pre-malignant lesions, and in the identification and removal of those agents that cause or contribute to cancer development. It is important to target initiators, co-carcinogens and promoters, since by removing any one of them, tumor growth may be prevented. Identification of these agents is difficult. Epidemiological studies largely study cancer after it has occurred. It would be preferable to identify potential carcinogenic substances at an earlier stage before they have caused a large number of malignancies and thus become identifiable by epidemiology. During the past three decades, we have accumulated an impressive amount of evidence concerning molecular pathways that when altered contribute to malignant growth. It is time that we start applying this knowledge to the identification of human carcinogens. Here, we review the molecular changes that are required for carcinogenesis and propose some criteria that, in the absence of epidemiological evidence, can be used to identify agents that cause or contribute to human cancer development. In the absence of epidemiological evidence, a given agent should be considered a human carcinogen when: (1) the agent causes or contributes to the development of tumors in animals that are of the same type as those tumors associated with exposure to the agent in humans; (2) the agent transforms or contributes to the transformation of human cells in culture and these cells are of the same type from which associated human malignancies arise; (3) there is molecular evidence that the agent interferes with one or more key molecular pathways in human cells which leads to the formation of human cancer.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15489132     DOI: 10.1016/j.semcancer.2004.06.002

Source DB:  PubMed          Journal:  Semin Cancer Biol        ISSN: 1044-579X            Impact factor:   15.707


  4 in total

Review 1.  Application of molecular technologies for phosphoproteomic analysis of clinical samples.

Authors:  M Pierobon; J Wulfkuhle; L Liotta; E Petricoin
Journal:  Oncogene       Date:  2014-03-10       Impact factor: 9.867

2.  Epigenetic effects and molecular mechanisms of tumorigenesis induced by cigarette smoke: an overview.

Authors:  Rong-Jane Chen; Louis W Chang; Pinpin Lin; Ying-Jan Wang
Journal:  J Oncol       Date:  2011-03-22       Impact factor: 4.375

3.  Conversion of a Non-Cancer-Selective Promoter into a Cancer-Selective Promoter.

Authors:  Praveen Bhoopathi; Anjan K Pradhan; Amit Kumar; Santanu Maji; Padmanabhan Mannangatti; Xiaoyan Deng; Dipankar Bandyopadhyay; Devanand Sarkar; Xiang-Yang Wang; Joseph W Landry; Swadesh K Das; Luni Emdad; Paul B Fisher
Journal:  Cancers (Basel)       Date:  2022-03-15       Impact factor: 6.575

4.  Effect of the accumulation of risk factors on the risk of oral squamous cell carcinoma

Authors:  Eduardo David Piemonte; Jerónimo Pablo Lazos; Paola Belardinelli; Graciela Del Valle Castillo; Angel Daniel Talavera; Dante Gustavo Secchi; Héctor Eduardo Lanfranchi Tizeira; Mabel Noemí Brunotto
Journal:  Rev Fac Cien Med Univ Nac Cordoba       Date:  2021-06-28
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.