التفاصيل البيبلوغرافية
| العنوان: |
Hexavalent Chromium Targets Securin to Drive Numerical Chromosome Instability in Human Lung Cells. |
| المؤلفون: |
Toyoda, Jennifer H.1 (AUTHOR) rspeer@salud.unm.edu, Martino, Julieta1 (AUTHOR) haiyan.lu@louisville.edu, Speer, Rachel M.1 (AUTHOR) joseph.kouokam@louisville.edu, Meaza, Idoia1 (AUTHOR), Lu, Haiyan1 (AUTHOR), Williams, Aggie R.1 (AUTHOR), Bolt, Alicia M.2 (AUTHOR) ambolt@salud.unm.edu, Kouokam, Joseph Calvin1 (AUTHOR), Aboueissa, Abou El-Makarim3 (AUTHOR), Wise Sr., John Pierce1 (AUTHOR) john.wise@louisville.edu |
| المصدر: |
International Journal of Molecular Sciences. Jan2024, Vol. 25 Issue 1, p256. 18p. |
| مصطلحات موضوعية: |
*HEXAVALENT chromium, *HUMAN chromosomes, *LUNGS, *DISEASE risk factors, *CENTROMERE, *CHROMOSOMES, *GENE amplification |
| مستخلص: |
Hexavalent chromium [Cr(VI)] is a known human lung carcinogen with widespread exposure in environmental and occupational settings. Despite well-known cancer risks, the molecular mechanisms of Cr(VI)-induced carcinogenesis are not well understood, but a major driver of Cr(VI) carcinogenesis is chromosome instability. Previously, we reported Cr(VI) induced numerical chromosome instability, premature centriole disengagement, centrosome amplification, premature centromere division, and spindle assembly checkpoint bypass. A key regulator of these events is securin, which acts by regulating the cleavage ability of separase. Thus, in this study we investigated securin disruption by Cr(VI) exposure. We exposed human lung cells to a particulate Cr(VI) compound, zinc chromate, for acute (24 h) and prolonged (120 h) time points. We found prolonged Cr(VI) exposure caused marked decrease in securin levels and function. After prolonged exposure at the highest concentration, securin protein levels were decreased to 15.3% of control cells, while securin mRNA quantification was 7.9% relative to control cells. Additionally, loss of securin function led to increased separase activity manifested as enhanced cleavage of separase substrates; separase, kendrin, and SCC1. These data show securin is targeted by prolonged Cr(VI) exposure in human lung cells. Thus, a new mechanistic model for Cr(VI)-induced carcinogenesis emerges with centrosome and centromere disruption as key components of numerical chromosome instability, a key driver in Cr(VI) carcinogenesis. [ABSTRACT FROM AUTHOR] |
| قاعدة البيانات: |
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