Targeting breast cancer: An overlook on current strategies

D Iacopetta, J Ceramella, N Baldino… - International Journal of …, 2023 - mdpi.com
Breast cancer (BC) is one of the most widely diagnosed cancers and a leading cause of
cancer death among women worldwide. Globally, BC is the second most frequent cancer …

Anti-breast cancer effects of phytochemicals: primary, secondary, and tertiary care

A Mazurakova, L Koklesova, M Samec, E Kudela… - EPMA Journal, 2022 - Springer
Breast cancer incidence is actually the highest one among all cancers. Overall breast cancer
management is associated with challenges considering risk assessment and predictive …

Machine learning-assisted prediction of the biological activity of aromatase inhibitors and data mining to explore similar compounds

M Ishfaq, M Aamir, F Ahmad, AM Mebed… - ACS omega, 2022 - ACS Publications
Designing molecules for drugs has been a hot topic for many decades. However, it is hard
and expensive to find a new molecule. Thus, the cost of the final drug is also increased …

Aromatase inhibitors for the treatment of breast cancer: An overview (2019–2023)

N Bhatia, S Thareja - Bioorganic Chemistry, 2024 - Elsevier
Aromatase inhibition is considered a legitimate approach for the treatment of ER-positive
(ER+) breast cancer as it accounts for more than 70% of breast cancer cases. Aromatase …

Novel pentacyclic derivatives and benzylidenes of the progesterone series cause anti-estrogenic and antiproliferative effects and induce apoptosis in breast cancer …

AM Scherbakov, SK Vorontsova, AI Khamidullina… - Investigational New …, 2023 - Springer
The promising antitumor effects of progesterone derivatives have been identified in many
studies. However, the specific mechanism of action of this class of compounds has not been …

Selective Estrogen receptor degraders (SERDs) for the treatment of breast cancer: An overview

N Bhatia, S Hazra, S Thareja - European Journal of Medicinal Chemistry, 2023 - Elsevier
Discovery of SERDs has changed the direction of anticancer research, as more than 70% of
breast cancer cases are estrogen receptor positive (ER+). Therapies such as selective …

Thiazole and related heterocyclic systems as anticancer agents: A review on synthetic strategies, mechanisms of action and SAR studies

Sahil, K Kaur, V Jaitak - Current medicinal chemistry, 2022 - benthamdirect.com
Background: Cancer is the second leading cause of death worldwide. Many anticancer
drugs are commercially available, but lack of selectivity, target specificity, cytotoxicity, and …

Design and synthesis of new 2-oxoquinoxalinyl-1, 2, 4-triazoles as antitumor VEGFR-2 inhibitors

M Zengin, OU Tan, RK Arafa, A Balkan - Bioorganic Chemistry, 2022 - Elsevier
VEGFR-2 is a tyrosine kinase receptor for VEGFs that play a central role in tumor
angiogenesis. The inhibition of the tyrosine kinase domain of VEGFR-2 has become an …

Conventional and new proposals of GnRH therapy for ovarian, breast, and prostatic cancers

MP Garrido, A Hernandez, M Vega, E Araya… - Frontiers in …, 2023 - frontiersin.org
For many years, luteinizing hormone-releasing hormone or gonadotropin-releasing
hormone (GnRH) analogs have been used to treat androgen or estrogen-dependent tumors …

Medicinal chemistry aspects and synthetic strategies of coumarin as aromatase inhibitors: an overview

P Ratre, S Kulkarni, S Das, C Liang, PK Mishra… - Medical Oncology, 2022 - Springer
Coumarin is a bicyclic oxygen bearing heterocyclic scaffold formed by fusion of benzene
with the pyrone ring. Because of its unique physicochemical characteristics and the ease …