AI Article Synopsis

  • Radiotherapy is a common treatment for breast cancer, but patients respond differently due to variations in their intrinsic radiosensitivity (RS). Researchers are exploring alternatives to the standard clonogenic assay for predicting RS.
  • In this study, blood samples from 10 breast cancer patients were analyzed using clonogenic, γ-H2AX, and apoptosis assays to evaluate their RS levels, revealing three distinct RS groups: high, medium, and low.
  • Results indicated that high RS patients had fewer double-strand breaks in their DNA, but their DNA repair systems were less active compared to others. The study concluded that using a combination of assays is necessary for more accurate predictions of intrinsic RS in breast cancer patients.

Article Abstract

Background: Radiotherapy is one of the routine treatment strategies for breast cancer (BC) patients. Different responses of the patient to radiation due to different intrinsic radiosensitivity (RS) were induced to the researcher try to introduce a standard assay for the prediction of RS. Clonogenic assay is recognized as a gold standard method in this subject but because of some of its disadvantages, it is needed for alternative assays. In this study, two assays were evaluated for this reason in ten BC patients with different RSs.

Methods: The peripheral blood of 10 volunteers with BC was obtained, and the peripheral blood mononuclear cells were extracted. After exposed with 2 Gy, survival fraction at 2 Gy (SF2) was calculated by clonogenic assay. γ-H2AX assay was performed for all patients, and apoptosis assay was evaluated for three represented categorized patients.

Results: RS of patients showed SF2 and categorized in three groups (high, medium, and low RS). Double-strand breaks (DSBs) were decreased in high radiosensitive patients, but the residual DSBs were clearly higher than other two groups. It is shown that the repair system in these patients is lower active than others. Apoptosis frequency in patient 4 is highly active which could induce the enhancement of her RS.

Conclusion: γ-H2AX and apoptosis assays could predict the intrinsic RS, but evaluation of them separately is not sufficient for this aim. It is necessary to consider all the parameters together and consideration of the combination of assays could fit a better prediction of intrinsic RS.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11296569PMC
http://dx.doi.org/10.4103/jmss.jmss_40_23DOI Listing

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