[HTML][HTML] Emerging systemic therapy options beyond CDK4/6 inhibitors for hormone receptor-positive HER2-negative advanced breast cancer

J Ma, JJ Chan, CH Toh, YS Yap - NPJ Breast Cancer, 2023 - nature.com
Endocrine therapy (ET) with cyclin-dependent kinase 4/6 inhibitor (CDK4/6i) is currently the
standard first-line treatment for most patients with hormone receptor (HR) positive, human …

[HTML][HTML] The evolving pathways of the efficacy of and resistance to CDK4/6 inhibitors in breast cancer

I Gomes, C Abreu, L Costa, S Casimiro - Cancers, 2023 - mdpi.com
Simple Summary Nowadays, the upfront treatment for patients facing a diagnosis of
advanced luminal breast cancer (BC) is a combination of endocrine therapy (ET) with an …

[HTML][HTML] CDK7 in breast cancer: mechanisms of action and therapeutic potential

Y Gong, H Li - Cell Communication and Signaling, 2024 - Springer
Abstract Cyclin-dependent kinase 7 (CDK7) serves as a pivotal regulator in orchestrating
cellular cycle dynamics and gene transcriptional activity. Elevated expression levels of …

[HTML][HTML] Selective CDK7 Inhibition Suppresses Cell Cycle Progression and MYC Signaling While Enhancing Apoptosis in Therapy-resistant Estrogen Receptor …

C Guarducci, A Nardone, D Russo, Z Nagy… - Clinical Cancer …, 2024 - AACR
Purpose: Resistance to endocrine therapy (ET) and CDK4/6 inhibitors (CDK4/6i) is a clinical
challenge in estrogen receptor (ER)-positive (ER+) breast cancer. Cyclin-dependent kinase …

[HTML][HTML] Recent advances in drug discovery for triple-negative breast cancer treatment

D Masci, C Naro, M Puxeddu, A Urbani, C Sette… - Molecules, 2023 - mdpi.com
Triple-negative breast cancer (TNBC) is one of the most heterogeneous and aggressive
breast cancer subtypes with a high risk of death on recurrence. To date, TNBC is very …

[HTML][HTML] Mechanisms of sensitivity and resistance to CDK4/CDK6 inhibitors in hormone receptor-positive breast cancer treatment

A Glaviano, SA Wander, RD Baird, KCH Yap… - Drug Resistance …, 2024 - Elsevier
Cell cycle dysregulation is a hallmark of cancer that promotes eccessive cell division. Cyclin-
dependent kinase 4 (CDK4) and cyclin-dependent kinase 6 (CDK6) are key molecules in …

Cyclin-dependent kinase 7 (CDK7) inhibitors as a novel therapeutic strategy for different molecular types of breast cancer

X Song, C Fang, Y Dai, Y Sun, C Qiu, X Lin… - British Journal of …, 2024 - nature.com
BACKGROUND Cyclin-dependent kinase (CDK) 7 is aberrantly overexpressed in many
types of cancer and is an attractive target for cancer therapy due to its dual role in …

Inhibition of cyclin-dependent kinase 7 mitigates doxorubicin cardiotoxicity and enhances anticancer efficacy

J Chen, J Wei, P Xia, Y Liu, MD Belew… - Cardiovascular …, 2024 - academic.oup.com
Aims The anthracycline family of anticancer agents such as doxorubicin (DOX) can induce
apoptotic death of cardiomyocytes and cause cardiotoxicity. We previously reported that …

[HTML][HTML] The BET PROTAC inhibitor GNE-987 displays anti-tumor effects by targeting super-enhancers regulated gene in osteosarcoma

D Wu, H Yin, C Yang, Z Zhang, F Fang, J Wang, X Li… - BMC cancer, 2024 - Springer
Background Osteosarcoma (OS) is one of the most common primary malignant tumors of
bone in children, which develops from osteoblasts and typically occurs during the rapid …

[HTML][HTML] Novel Treatment Strategies for Hormone Receptor (HR)-Positive, HER2-Negative Metastatic Breast Cancer

A Ferro, M Campora, A Caldara, D De Lisi… - Journal of Clinical …, 2024 - mdpi.com
Estrogen receptor (ER)-positive breast cancer (BC) is the most common BC subtype.
Endocrine therapy (ET) targeting ER signaling still remains the mainstay treatment option for …