Multiomic analysis of cytokines in immuno-oncology

V Jurisic - Expert review of proteomics, 2020 - Taylor & Francis
Introduction: Cytokines are a diverse group of peptides produced by different cell types
including cancer cells and various subpopulations of immune system cells. They exert their …

Mechanisms of acquired BRAF inhibitor resistance in melanoma: a systematic review

I Proietti, N Skroza, N Bernardini, E Tolino, V Balduzzi… - Cancers, 2020 - mdpi.com
Simple Summary Patients with advanced melanoma are often treated with v-raf murine
sarcoma viral oncogene homolog B1 (BRAF) inhibitors. Although these agents prolong life …

BRAF gene and melanoma: Back to the future

M Ottaviano, EF Giunta, M Tortora, M Curvietto… - International Journal of …, 2021 - mdpi.com
As widely acknowledged, 40–50% of all melanoma patients harbour an activating BRAF
mutation (mostly BRAF V600E). The identification of the RAS–RAF–MEK–ERK (MAP kinase) …

CDK9 inhibition constrains multiple oncogenic transcriptional and epigenetic pathways in prostate cancer

R Rahman, MH Rahaman, AR Hanson, N Choo… - British Journal of …, 2024 - nature.com
Background Cyclin-dependent kinase 9 (CDK9) stimulates oncogenic transcriptional
pathways in cancer and CDK9 inhibitors have emerged as promising therapeutic …

CSN6 promotes melanoma proliferation and metastasis by controlling the UBR5-mediated ubiquitination and degradation of CDK9

Y Zhang, J Hou, S Shi, J Du, Y Liu, P Huang, Q Li… - Cell Death & …, 2021 - nature.com
As a critical subunit of the constitutive photomorphogenesis 9 (COP9) signalosome (CSN),
CSN6 is upregulated in some human cancers and plays critical roles in tumorigenesis and …

Characterization of vemurafenib-resistant melanoma cell lines reveals novel hallmarks of targeted therapy resistance

M Radić, I Vlašić, M Jazvinšćak Jembrek… - International journal of …, 2022 - mdpi.com
Regardless of the significant improvements in treatment of melanoma, the majority of
patients develop resistance whose mechanisms are still not completely understood. Hence …

[HTML][HTML] The mechanism and consequences of BRAF inhibitor resistance in melanoma

K Golub, W Bai, Z Zhang, H Xiao, R Sun, J Shen… - Genome Instability & …, 2023 - Springer
Abstract BRAF V600E is a constitutive BRAF (B-raf proto-oncogene, serine/threonine
kinase) mutation that accounts for more than 90% of BRAF mutations in melanoma …

The epigenetic regulation of cancer cell recovery from therapy exposure and its implications as a novel therapeutic strategy for preventing disease recurrence

CO Appiah, M Singh, L May, I Bakshi… - Advances in Cancer …, 2023 - Elsevier
The ultimate goal of cancer therapy is the elimination of disease from patients. Most directly,
this occurs through therapy-induced cell death. Therapy-induced growth arrest can also be a …

[HTML][HTML] In vivo vulnerabilities to GPX4 and HDAC inhibitors in drug-persistent versus drug-resistant BRAFV600E lung adenocarcinoma

MJ Nokin, E Darbo, E Richard, S San José… - Cell Reports …, 2024 - cell.com
The current targeted therapy for BRAF V600E-mutant lung cancer consists of a dual
blockade of RAF/MEK kinases often combining dabrafenib/trametinib (D/T). This regimen …

Role of Histone Deacetylase 6 and Histone Deacetylase 6 Inhibition in Colorectal Cancer

A Vuletić, K Mirjačić Martinović, J Spasić - Pharmaceutics, 2023 - mdpi.com
Histone deacetylase 6 (HDAC6), by deacetylation of multiple substrates and association
with interacting proteins, regulates many physiological processes that are involved in cancer …