Diazo-coupling reaction between 2-aminothiazole and thymol; Synthesis, DFT studies, and specific heat capacity calculations using TGA-DSC.

Abstract

This study was aimed to investigate the role of E2F1 in breast cancer biology. Expression of E2F1, a transcription factor of many oncogenes and tumor suppressor genes, is lowered in several malignancies including breast carcinoma. In the present study we analyzed the status of E2F1 expression in association with diverse attributes of breast malignancy and its impact on cancer progression. For this purpose we used various freely available online applications for gene enrichment, expression and methylation analysis, to extract mutation based E2F1 map, to measure E2F1 drug sensitivity and to determine E2F1 association with damage response proteins. Results revealed tissue specific regulatory behavior of E2F1. Moreover, the key role of E2F1 in the promotion of metastasis, stem cell mediated carcinogenesis, estrogen mediated cell proliferation and cellular defense system has therefore highlighted it as metaplastic marker and hot member of key resistome pathways. The information thus generated can be employed for future implications in devising rational therapeutic strategies. Moreover, this study has provided a more detailed insight into the diagnostic and prognostic potential of E2F.