Molecular fingerprints of environmental carcinogens in human cancer
C Ceccaroli1, A Pulliero, M Geretto
1a Department of Health Sciences, University of Genoa , Italy.
Abstract:
Identification of specific molecular changes (fingerprints) is important to identify cancer etiology. Exploitable biomarkers are related to DNA, epigenetics, and proteins. DNA adducts are the turning point between environmental exposures and biological damage. DNA mutational fingerprints are induced by carcinogens in tumor suppressor and oncogenes. In an epigenetic domain, methylation changes occurs in specific genes for arsenic, benzene, chromium, and cigarette smoke. Alteration of specific microRNA has been reported for environmental carcinogens. Benzo(a)pyrene, cadmium, coal, and wood dust hits specific heat-shock proteins and metalloproteases. The multiple analysis of these biomarkers provides information on the carcinogenic mechanisms activated by exposure to environmental carcinogens.
Insights
Identifying molecular fingerprints like DNA adducts and epigenetic changes is key to understanding cancer causes from environmental exposures. Analyzing these biomarkers reveals carcinogen-induced damage and mechanisms.
Area of Science:
- Environmental Health Sciences
- Molecular Biology
- Cancer Research
Background:
- Identifying specific molecular changes, or fingerprints, is crucial for determining cancer etiology.
- Biomarkers for cancer research include DNA, epigenetic modifications, and proteins.
- DNA adducts represent a critical link between environmental exposures and subsequent biological damage.
Purpose of the Study:
- To explore the role of molecular fingerprints in identifying cancer causes.
- To highlight exploitable biomarkers in DNA, epigenetics, and proteins.
- To understand the mechanisms of carcinogenesis activated by environmental carcinogens.
Main Methods:
- Analysis of DNA adducts and mutational fingerprints induced by carcinogens.
- Assessment of epigenetic changes, such as gene methylation, linked to specific environmental agents (arsenic, benzene, chromium, cigarette smoke).
- Investigation of microRNA alterations and protein modifications (heat-shock proteins, metalloproteases) associated with environmental carcinogens (benzo(a)pyrene, cadmium, coal, wood dust).
Main Results:
- Carcinogens induce specific DNA mutational fingerprints in critical genes.
- Environmental exposures like arsenic, benzene, chromium, and cigarette smoke are associated with distinct gene methylation patterns.
- Specific environmental carcinogens impact particular microRNAs, heat-shock proteins, and metalloproteases.
Conclusions:
- Molecular fingerprints derived from DNA, epigenetics, and proteins serve as valuable indicators of environmental carcinogen exposure and action.
- The comprehensive analysis of these diverse biomarkers provides insights into the molecular pathways underlying environmentally induced cancers.
- Understanding these mechanisms is essential for developing targeted prevention and intervention strategies against environmental carcinogens.
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