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Further Analytical Studies on a Mercuri Thiol Adduct Isolated from a Human Prostate Cancer Cell Line (LNCaP)

DOI: 10.4236/jasmi.2022.123003, PP. 31-47

Keywords: Low Molecular Weight Thiol, Conthiol, LNCaP Prostate Tumour Cell Line, Thiol Adduct Analysis, LC-MS Analysis, ICP-MS Analysis

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Abstract:

Thiols play vital roles in cellular metabolism knowledge of which may be important in the design of future anticancer drugs. Previous work on the composition of the thiols present in human cancer cell lines has shown the presence of an unknown low molecular weight species, deemed to be a Conthiol”, which could be important in this respect. This was prepared and isolated from a human prostate cancer cell line (LNCaP) in the form of an adduct of 2-mercuri-4-nitrophenol; it accounts for 56.5% of the total cellular thiols present in this cell line. Initial LC-MS analysis of this adduct had indicated that the possible molecular weight of the thiol was in the region of 467 daltons. In further analytical studies to identify the thiol, attempts were made to release it from the adduct by passage through a Thiopropyl Sepharose6B column. LC-MS analysis of the column eluate revealed two components yielding negative ion fragments of 427 m/z and 449 m/z. Only the former component contained thiol, indicating that a breakdown and/or possible rearrangement of the Conthiol had occurred. Further investigations of the column thiol eluate using ICP-MS analysis showed that the sulfur content agreed with the spectrophotometric analysis result (Ellman assay) and that the molecule did not contain phosphate. Amino acid analyses of the eluate were negative. In an attempt to prevent the breakdown of the thiol released by the Thiopropyl Sepharose 6B column, the adduct was treated with 5% v/v bromine water prior to applying to the column. In this instance the thiol containing eluate obtained from the column was treated

References

[1]  [1]Giles, G.I. (2006) The Redox Regulationof Thiol Dependant Signaling Pathways in Cancer. Current Pharmaceutical Design, 12, 4427-4443.
https://doi.org/10.2174/138161206779010549
[2]  Winterbourn, C.C. and Hampton, M.B. (2008) Thiol Chemistry and Specificity in Redox Signaling. Free Radical Biology and Medicine, 45, 549-561.
https://doi.org/10.1016/j.freeradbiomed.2008.05.004
[3]  Harris, I.S., et al. (2015) Glutathione and Thioredoxin Antioxidant Pathways Synergize to Drive Cancer Initiation and Progression. Cancer Cell, 27, 211-222.
https://doi.org/10.1016/j.ccell.2014.11.019
[4]  Gronow, M. (2018) Cellular Protein Thiols: Studies on Human Prostate Cell Lines; A Lymph Node Cancer Line (LNCaP) and a Virally Transformed Normal Cell Line (PNT2). Oncology Research and Reviews, 1, 1-6.
https://doi.org/10.15761/ORR.1000116
[5]  Gronow, M. (2020) Isolation and Analysis of a Non-Protein Low Molecular Weight thiol-Mercurial Adduct from Human Prostate Lymph Node Cells (LNCaP). Bioscience Reports, 40, BSR20201343.
https://doi.org/10.1042/BSR20201343
[6]  Ellman, G.L. (1959) Tissue Sulfhydryl Groups. Archives of Biochemistry and Biophysics, 82, 70-77.
https://doi.org/10.1016/0003-9861(59)90090-6
[7]  Gronow, M. (2010) Studies on the Non-Protein Thiols of a Human Prostatic Cancer Cell Line: Glutathione Content. Cancers, 2, 1092-1106.
https://doi.org/10.3390/cancers2021092
[8]  Gronow, M. (2020) Studies on the Thiol Components of Isolated Nuclei. Journal of Analytical Sciences, Methods and Instrumentation, 10, 36-42.
https://doi.org/10.4236/jasmi.2020.101003

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