References
- Oussama MNK, Atord M. Guidelines for the early detection and screening of breast cancer. World Health Organization (EMRO30) 30, 1–55 (2008).
- Waks AG, Winer EP. Breast cancer treatment: a review. JAMA 321(3), 288–300 (2019).
- Loibl S, Poortmans P, Morrow M, Denkert C, Curigliano G. Epidemiology and risk factors. Lancet 397, 1750–1769 (2021).
- Harbeck N, Burstein HJ, Hurvitz SA, Johnston S, Vidal GA. A look at current and potential treatment\approaches for hormone receptor-positive, HER2-negative early breast cancer. Cancer 128, 2209–2223 (2022).
- Tong CW, Wu M, Cho W, To KK. Recent advances in the treatment of breast cancer. Front. Oncol. 8, 381990 (2018).
- McAndrew NP, Finn RS. Clinical review on the management of hormone receptor-positive metastatic breast cancer. JCO Oncol. Pract. 18(5), 319–327 (2022).
- Arora S, Narayan P, Osgood CL et al. US FDA drug approvals for breast cancer: a decade in review. Clin. Cancer Res. 28(6), 1072–1086 (2022).
- An J, Peng C, Xie X, Peng F. New advances in targeted therapy of HER2-negative breast cancer. Front. Oncol. 12, 828438 (2022).
- Cui W, Aouidate A, Wang S, Yu Q, Li Y, Yuan S. Discovering anti-cancer drugs via computational methods. Front. Pharmacol. 11, 733 (2020).
- Quijia CR, Chorilli M. Piperine for treating breast cancer: a review of molecular mechanisms, combination with anticancer drugs, and nanosystems. Phytother. Res. 36(1), 147–163 (2022).
- Veazey K. What to know about anthracycline chemotherapy Medical News Today (2022). www.medicalnewstoday.com/articles/anthracycline-chemotherapy#how-effective-is-it
- Breastcancer.org. Anthracycline chemo regimen seems better than regimen without anthracycline for early-stage, HER2-negative, high-risk disease (2016). www.breastcancer.org/research-news/chemo-w-anthracycline-better-for-some
- Anthracyclines side effects and late effects (no date). www.idc-online.com/technical_references/pdfs/chemical_engineering/Anthracyclines_Side_Effects_and_Late_Effects.pdf
- Venkateah P, Kasi A. Anthracyclines. In: StatPearls. FL, USA (2022). www.ncbi.nlm.nih.gov/books/NBK538187/
- Petrou A, Fesatidou M, Geronikaki A. Thiazole ring – a biologically active scaffold. Molecules 26(11), 3166 (2021).
- Scott KA, Njardarson JT. Analysis of US FDA-approved drugs containing sulfur atoms. Sulfur Chemistry 1(1), 1–34 (2019).
- Sharma PC, Bansal KK, Sharma A, Sharma D, Deep A. Thiazole-containing compounds as therapeutic targets for cancer therapy. Eur. J. Med. Chem. 188, 112016 (2020).
- Pola S. Significance of thiazole-based heterocycles for bioactive systems. In: Scope of Selective Heterocycles from Organic and Pharmaceutical Perspective. Varala R ( Ed.). Janeza Trdine 9, 51000, Riieka, Coratia, 13–62 (2016).
- Zheng S, Zhong Q, Xi Y et al. Modification and biological evaluation of thiazole derivatives as novel inhibitors of metastatic cancer cell migration and invasion. J. Med. Chem. 57(15), 6653–6667 (2014).
- Makam P, Thakur PK, Kannan T. In vitro and in silico antimalarial activity of 2-(2-hydrazinyl)thiazole derivatives. Eur. J. Pharm. Sci. 52, 138–145 (2014).
- Dey S, Das A, Yadav RN et al. Visible light-induced ternary electron donor–acceptor complex enabled synthesis of 2-(2-hydrazinyl) thiazole derivatives and the assessment of their antioxidant and antidiabetic therapeutic potential. Org. Biomol. Chem. 21(8), 1771–1779 (2023).
- Jadav SS, Kaptein S, Timiri A et al. Design, synthesis, optimization and antiviral activity of a class of hybrid dengue virus E protein inhibitors. Bioorg. Med. Chem. Lett. 25(8), 1747–1752 (2015).
- Alsharekh MM, Althagafi II, Shaaban MR, Farghaly TA. Microwave-assisted and thermal synthesis of nanosized thiazolyl-phenothiazine derivatives and their biological activities. Res. Chem. Intermed. 45, 127–154 (2019).
- Yurttaş L, Çavuşoğlu BK, Cantürk Z. Novel 2-(2-hydrazinyl) thiazole derivatives as chemotherapeutic agents. Synthetic Communications 50(20), 3072–3079 (2020).
- de Santana TI, de Oliveira BM, de Moraes GPAT et al. Synthesis, anticancer activity and mechanism of action of new thiazole derivatives. Eur. J. Med. Chem. 144, 874–886 (2018).
- Filimonov AS, Chepanova AA, Luzina OA et al. New hydrazinothiazole derivatives of usnic acid as potent Tdp1 inhibitors. Molecules 24(20), 3711 (2019).
- Zakharenko AL, Luzina OA, Sokolov DN et al. Novel tyrosyl-DNA phosphodiesterase 1 inhibitors enhance the therapeutic impact of topotecan on in vivo tumor models. Eur. J. Med. Chem. 161, 581–593 (2019).
- Chimenti F, Bizzarri B, Maccioni E et al. A novel histone acetyltransferase inhibitor modulating Gcn5 network: cyclopentylidene-[4-(4′-chlorophenyl)thiazol-2-yl) hydrazone. J. Med. Chem. 52(2), 530–536 (2009).
- Zaki I, Abdelhameid MK, El-Deen IM, Wahab AHAA, Ashmawy AM, Mohamed KO. Design, synthesis and screening of 1,2,4-triazinone derivatives as potential antitumor agents with apoptosis inducing activity on MCF-7 breast cancer cell line. Eur. J. Med. Chem. 156, 563–579 (2018).
- Fantacuzzi M, De Filippis B, Gallorini M et al. Synthesis, biological evaluation, and docking study of indole aryl sulfonamides as aromatase inhibitors. Eur. J. Med. Chem. 185, 111815 (2020).
- Blackburn HL, Ellsworth DL, Shriver CD, Ellsworth RE. Role of cytochrome P450 genes in breast cancer etiology and treatment: effects on estrogen biosynthesis, metabolism and response to endocrine therapy. Cancer Causes Control 26, 319–332 (2015).
- Long JR, Kataoka N, Shu XO et al. Genetic polymorphisms of the CYP19A1 gene and breast cancer survival. Cancer Epidemiol. Biomarkers Prev. 15(11), 2115–2122 (2006).
- Butti R, Das S, Gunasekaran VP, Yadav AS, Kumar D, Kundu GC. Receptor tyrosine kinases (RTKs) in breast cancer: signaling, therapeutic implications and challenges. Mol. Cancer 17(1), 1–18 (2018).
- Ghosh D, Egbuta C, Lo J. Testosterone complex and non-steroidal ligands of human aromatase. J. Steroid Biochem. Mol. Biol. 181, 11–19 (2018).
- Tong L, Warren TC, King J, Betageri R, Rose J, Jakes S. Crystal structures of the human p56lckSH2 domain in complex with two short phosphotyrosyl peptides at 1.0 Å and 1.8 Å resolution. J. Mol. Biol. 256(3), 601–610 (1996).
- Thomsen R, Christensen MH. MolDock: a new technique for high-accuracy molecular docking. J. Med. Chem. 49(11), 3315–3321 (2006).
- Secci D, Carradori S, Bizzarri B et al. Synthesis of a novel series of thiazole-based histone acetyltransferase inhibitors. Bioorg. Med. Chem. 22(5), 1680–1689 (2014).
- Kaminskyy D, Kryshchyshyn A, Lesyk R. 5-Ene-4-thiazolidinones – an efficient tool in medicinal chemistry. Eur. J. Med. Chem. 140, 542–594 (2017).
- Kheirollahi A, Pordeli M, Safavi M, Mashkouri S, Naimi-Jamal MR, Ardestani SK. Cytotoxic and apoptotic effects of synthetic benzochromene derivatives on human cancer cell lines. Naunyn Schmiedebergs Arch. Pharmacol. 387, 1199–1208 (2014).
- Mohammed FZ, Rizzk YW, El Deen IM et al. Design, synthesis, cytotoxic screening and molecular docking studies of novel hybrid thiosemicarbazone derivatives as anticancer agents. Chem. Biodivers. 18(12), e2100580 (2021).
- Mohammed FZ, Rizzk YW, El-Deen IM et al. Discovery of 2-amino-4H-1,3,4-thiadiazine-5 (6H)-one derivatives and their in vitro antitumor investigation. ChemistrySelect 7(7), e202104333 (2022).
- Wu CS, Chen J, Chen JJW et al. Terpinen-4-01 induces apoptosis in human normal cell lung cancer in vitro and in vivo. Evid. Based Complement. Altern. Med. 2012, 818261 (2012).