Systemic therapy for hormone receptor‐positive/human epidermal growth factor receptor 2‐negative early stage and metastatic breast cancer

LA Huppert, O Gumusay, D Idossa… - CA: a cancer journal for …, 2023 - Wiley Online Library
Hormone receptor (HR)‐positive and human epidermal growth factor receptor 2 (HER2)‐
negative breast cancer is defined by the presence of the estrogen receptor and/or the …

Natural killer cells in cancer biology and therapy

SY Wu, T Fu, YZ Jiang, ZM Shao - Molecular cancer, 2020 - Springer
The tumor microenvironment is highly complex, and immune escape is currently considered
an important hallmark of cancer, largely contributing to tumor progression and metastasis …

Breast cancer treatments: updates and new challenges

A Burguin, C Diorio, F Durocher - Journal of personalized medicine, 2021 - mdpi.com
Breast cancer (BC) is the most frequent cancer diagnosed in women worldwide. This
heterogeneous disease can be classified into four molecular subtypes (luminal A, luminal B …

PI3K/AKT/mTOR-targeted therapy for breast cancer

K Zhu, Y Wu, P He, Y Fan, X Zhong, H Zheng, T Luo - Cells, 2022 - mdpi.com
Phosphatidylinositol 3-kinase (PI3K), protein kinase B (PKB/AKT) and mechanistic target of
rapamycin (mTOR)(PAM) pathways play important roles in breast tumorigenesis and confer …

An emerging generation of endocrine therapies in breast cancer: a clinical perspective

R Patel, P Klein, A Tiersten, JA Sparano - NPJ Breast Cancer, 2023 - nature.com
Anti-estrogen therapy is a key component of the treatment of both early and advanced-stage
hormone receptor (HR)-positive breast cancer. This review discusses the recent emergence …

Fulvestrant plus capivasertib versus placebo after relapse or progression on an aromatase inhibitor in metastatic, oestrogen receptor-positive breast cancer (FAKTION …

RH Jones, A Casbard, M Carucci, C Cox… - The Lancet …, 2020 - thelancet.com
Background Capivasertib (AZD5363) is a potent selective oral inhibitor of all three isoforms
of the serine/threonine kinase AKT. The FAKTION trial investigated whether the addition of …

ESR1 mutations in breast cancer

D Dustin, G Gu, SAW Fuqua - Cancer, 2019 - Wiley Online Library
The acquisition of ligand‐independent ESR1 mutations during aromatase inhibitor therapy
in metastatic estrogen receptor (ER)‐positive breast cancer is a common mechanism of …

Targeting mTOR and metabolism in cancer: lessons and innovations

C Magaway, E Kim, E Jacinto - Cells, 2019 - mdpi.com
Cancer cells support their growth and proliferation by reprogramming their metabolism in
order to gain access to nutrients. Despite the heterogeneity in genetic mutations that lead to …

Targeting the PI3K/AKT/mTOR pathway in hormone-positive breast cancer

SE Nunnery, IA Mayer - Drugs, 2020 - Springer
Approximately 70% of invasive breast cancers have some degree of dependence on the
estrogen hormone for cell proliferation and growth. These tumors have estrogen and/or …

Drugging the PI3K/AKT/mTOR pathway in ER+ breast cancer

CL Alves, HJ Ditzel - International Journal of Molecular Sciences, 2023 - mdpi.com
The frequent activation of the PI3K/AKT/mTOR pathway and its crucial role in estrogen
receptor-positive (ER+) breast cancer tumorigenesis and drug resistance has made it a …