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. Author manuscript; available in PMC: 2024 Sep 5.
Published in final edited form as: J Environ Health. 2023 Dec;86(5):30–35.

TABLE 2.

Genotoxic Endpoints for Six Metals

Chromium-6 (Cr6+) Arsenic (As) Nickel (Ni) Lead (Pb) Mercury (Hg) Zinc (Zn)
National Toxicology Program classification 1 1 1 (Ni compounds) 2 3 3
Substance Priority List rank 17 1 58 2 3 75
Chromosomal damage *
DNA methylation *
DNA–protein cross-linking
Micronuclei formation *
Sister-chromatid exchange
DNA repair inhibition
Gene mutation *
Chromosomal aberrations *
DNA fragmentation *
DNA strand breaks *
Telomere alteration
*

Represents some studies with preventive effects.

Note. Table 1 presents the number of published studies that identified the genotoxic endpoint from a search of toxicological profiles and literature using PubMed conducted on October 17, 2022. Search terms included: endpoint induced by X metal exposure (e.g., telomere alteration induced by arsenic metal exposure, only lead and zinc were searched as Pb and Zn). The shading is based on the number of given genotoxic endpoints studied: green = 1–10; yellow = 11–24; and red = >24. A lack of shading indicates no studies were found. For the National Toxicology Program classification: 1 = known carcinogen; 2 = reasonably anticipated to be a human carcinogen; and 3 = not classified by the National Toxicology Program. For the Substance Priority List rank: 1 represents the highest priority. The only form of chromium classified as carcinogenic to humans is hexavalent chromium (Cr6+).