PI3K inhibitors are finally coming of age

B Vanhaesebroeck, MWD Perry, JR Brown… - Nature reviews Drug …, 2021 - nature.com
Abstract Overactive phosphoinositide 3-kinase (PI3K) in cancer and immune dysregulation
has spurred extensive efforts to develop therapeutic PI3K inhibitors. Although progress has …

At a crossroads: how to translate the roles of PI3K in oncogenic and metabolic signalling into improvements in cancer therapy

N Vasan, LC Cantley - Nature Reviews Clinical Oncology, 2022 - nature.com
Numerous agents targeting various phosphatidylinositol 3-kinase (PI3K) pathway
components, including PI3K, AKT and mTOR, have been tested in oncology clinical trials …

The present and future of PI3K inhibitors for cancer therapy

P Castel, E Toska, JA Engelman, M Scaltriti - Nature cancer, 2021 - nature.com
Abstract Phosphoinositide 3-kinase (PI3K) signaling regulates cellular proliferation, survival
and metabolism, and its aberrant activation is one of the most frequent oncogenic events …

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 …

Self‐stabilized supramolecular assemblies constructed from PEGylated dendritic peptide conjugate for augmenting tumor retention and therapy

X Zheng, D Pan, X Chen, L Wu, M Chen… - Advanced …, 2021 - Wiley Online Library
Supramolecular self‐assemblies of dendritic peptides with well‐organized nanostructures
have great potential as multifunctional biomaterials, yet the complex self‐assembly …

Dysregulated amino acid sensing drives colorectal cancer growth and metabolic reprogramming leading to chemoresistance

S Solanki, K Sanchez, V Ponnusamy, V Kota, HN Bell… - Gastroenterology, 2023 - Elsevier
Background & Aims Colorectal cancer (CRC) is a devastating disease that is highly
modulated by dietary nutrients. Mechanistic target of rapamycin complex 1 (mTORC1) …

AKT-mTORC1 reactivation is the dominant resistance driver for PI3Kβ/AKT inhibitors in PTEN-null breast cancer and can be overcome by combining with Mcl-1 …

S Dunn, C Eberlein, J Yu, A Gris-Oliver, SH Ong… - Oncogene, 2022 - nature.com
The PI3K pathway is commonly activated in breast cancer, with PI3K-AKT pathway inhibitors
used clinically. However, mechanisms that limit or enhance the therapeutic effects of PI3K …

Phosphoinositide 3-kinase (PI3K) inhibitors and breast cancer: an overview of current achievements

A Bertucci, F Bertucci, A Gonçalves - Cancers, 2023 - mdpi.com
Simple Summary Breast cancer remains the fourth-leading cause of death worldwide, and
therapeutic improvement is warranted. The phosphatidylinositol 3-kinase (PI3K) pathway is …

Genomic analysis of cervical carcinoma identifies Alpelisib as a therapeutic option for PIK3CA‐mutant cervical carcinoma via the PI3K/AKT pathway

Y Wei, S Lin, W Zhi, T Chu, B Liu, T Peng… - Journal of Medical …, 2023 - Wiley Online Library
Cervical carcinoma is a serious type of gynecological cancer that can affect women of all
ages. Cervical carcinoma presents challenges for precision medicine, as not all tumors have …

The role of TSC2 in breast cancer: a literature review

QY Zhu, ZM He, WM Cao, B Li - Frontiers in Oncology, 2023 - frontiersin.org
TSC2 is a tumor suppressor gene as well as a disease-causing gene for autosomal
dominant disorder tuberous sclerosis complex (TSC). Research has found that some tumor …