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May 17, 20260 citationsOpen Access

Growth Inhibitory Effects of Engineered Thionucleosides in McF-7 Breast Cancer Cells

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EPElena Sergeyevna Petrova

Key Points

  • Evaluate the growth inhibitory effects of engineered thionucleosides on MCF-7 breast cancer cells.
  • Examined modified nitrogen bases and nucleosides for anticancer properties.
  • Utilized antiproliferative assay to assess growth inhibition in MCF-7 cell line.
  • 2-mercaptopurine led to 40% inhibition of growth in MCF-7 cells.
  • Nitrogen bases exhibited potential antibacterial properties against MCF-7 cells.

Abstract

The MCF-7 cell line, a well-researched human breast cancer model, has significantly contributed to advancing our knowledge of breast cancer biology and innovating treatment approaches. A notable trait of MCF-7 cells is their responsiveness to estrogen. Research involving MCF-7 cells has yielded significant knowledge regarding hormone receptor signaling and the modes of operation of anti-estrogen treatments like tamoxifen. Furthermore, MCF-7 cells have served as a platform for investigating drug resistance and for identifying prospective anti-cancer agents 1. Modified nitrogen bases 2-mercaptopurine, thioguanine, and nucleosides 6-thioguanosine and 2’-deoxy-6-thioguanosine, along with DesulfatedAztreonam and 2- (Benzylsulfanyl) -1-hydroxyadenosine, were evaluated for their potential anticancer properties. The antiproliferative assay was utilized to examine the characteristics of MCF-7 cells. The findings indicated that 2-mercaptopurine exhibited notable efficacy against MCF-7 cells, resulting in a 40% inhibition of growth 4. Treatment with nitrogen bases 2-mercaptopurine and 6-thioguanine, along with nucleosides 6-thioguanosine and 2’-deoxy-6-thioguanosine, may exhibit antibacterial properties against MCF-7. Our findings offer fresh perspectives on the cytotoxic efficacy of thiopurines and propose a justification for opting for mercaptopurine over thioguanine in addressing various bacterialinduced illnesses.

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Elena Sergeyevna Petrova (2026) studied this question.

synapsesocial.com/papers/6a095b1b7880e6d24efe0e4bhttps://doi.org/10.5281/zenodo.20205427
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