Literature DB >> 2654303

Human melanocytic neoplasms and their etiologic relationship with sunlight.

D E Elder1.   

Abstract

Two hypotheses have been presented. The first states that melanomas commonly evolve from normal melanocytes by a tumor progression pathway from a banal nevus to a nevus with dysplasia, to a micro-invasive, and then to a fully evolved, tumorigenic, primary melanoma which has competence for metastasis. It is important to note that not all melanomas follow this complete pathway. As Foulds noted long ago, tumors may bypass any of the stages of tumor progression. Thus, many melanomas do not, apparently, arise in nevi, and melanomas may evolve "fully formed" as pure tumorigenic nodules. However, from the biological point of view, study of the benign potential precursors (nevi and, especially, dysplastic nevi as well as microinvasive melanomas) may well reveal mechanisms of progression that are applicable to all melanomas, and perhaps to other solid tumors as well. From a clinical viewpoint, follow-up and education of patients at increased risk for melanoma, and early diagnosis of melanomas in their curable, microinvasive stages may result in a reduction of mortality from the disease, even without influencing its overall incidence. The melanomas that occur on plantar and palmar (acral) skin appear to progress through a microinvasive stage similar to that of other cutaneous melanomas. However, the significance of precursor and marker lesions (if any exist) in acral melanoma remains to be elucidated by clinicopathologic and epidemiologic studies. The possibility of etiologic agents other than UV light, such as chemical carcinogens and/or viruses, should be investigated in these cases. The second hypothesis presented here, that UV light is etiologic for the common cutaneous melanoma of white populations, has support from clinical, epidemiologic, and biologic observations. From a biologic viewpoint, ultraviolet light has all of the properties that might enable it to act as a complete carcinogen, and to enhance tumor progression in melanocytic "potential-precursor" lesions. Clinically, it seems appropriate to encourage patients (and members of the general population, as well) to adopt sensible attitudes to sun exposure. By such means, it is possible that some melanomas might be prevented, or that the rate and incidence of progression to more-advanced stages might be inhibited.

Entities:  

Mesh:

Year:  1989        PMID: 2654303     DOI: 10.1111/1523-1747.ep13076732

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN: 0022-202X            Impact factor:   8.551


  11 in total

1.  Genomic instability in radial growth phase melanoma cell lines after ultraviolet irradiation.

Authors:  M R Hussein; A K Haemel; O Sudilovsky; G S Wood
Journal:  J Clin Pathol       Date:  2005-04       Impact factor: 3.411

2.  Nevi and migration within the United States and Canada: a population-based cross-sectional study.

Authors:  L K Dennis; E White; B McKnight; A Kristal; J A Lee; P Odland
Journal:  Cancer Causes Control       Date:  1996-07       Impact factor: 2.506

3.  Self screening for risk of melanoma: validity of self mole counting by patients in a single general practice.

Authors:  P Little; M Keefe; J White
Journal:  BMJ       Date:  1995-04-08

4.  Acral Lentigines, Is it a Paraneoplastic Syndrome?

Authors:  Saad Al Mohizea; Amal Al-Balbeesi
Journal:  Int J Health Sci (Qassim)       Date:  2009-01

5.  Recent cohort trends in malignant melanoma by anatomic site in the United States.

Authors:  L K Dennis; E White; J A Lee
Journal:  Cancer Causes Control       Date:  1993-03       Impact factor: 2.506

6.  Localization of a putative tumor suppressor gene by using homozygous deletions in melanomas.

Authors:  J Weaver-Feldhaus; N A Gruis; S Neuhausen; D Le Paslier; E Stockert; M H Skolnick; A Kamb
Journal:  Proc Natl Acad Sci U S A       Date:  1994-08-02       Impact factor: 11.205

7.  Genetic predisposition of transgenic mouse melanocytes to melanoma results in malignant melanoma after exposure to a low ultraviolet B intensity nontumorigenic for normal melanocytes.

Authors:  L Larue; N Dougherty; B Mintz
Journal:  Proc Natl Acad Sci U S A       Date:  1992-10-15       Impact factor: 11.205

8.  A theory of site distribution of melanomas: Queensland, Australia.

Authors:  A Green
Journal:  Cancer Causes Control       Date:  1992-11       Impact factor: 2.506

9.  Chronic growth stimulation of human adult melanocytes by inflammatory mediators in vitro: implications for nevus formation and initial steps in melanocyte oncogenesis.

Authors:  E E Medrano; J Z Farooqui; R E Boissy; Y L Boissy; B Akadiri; J J Nordlund
Journal:  Proc Natl Acad Sci U S A       Date:  1993-03-01       Impact factor: 11.205

10.  Langerhans cell migration patterns from sheep skin following topical application of carcinogens.

Authors:  S J Ragg; G W Dandie; G M Woods; P J O'Connell; H K Muller
Journal:  Int J Exp Pathol       Date:  1994-02       Impact factor: 1.925

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.