From seabed to bedside: A review on promising marine anticancer compounds

E Wang, MA Sorolla, PD Gopal Krishnan, A Sorolla - Biomolecules, 2020 - mdpi.com
The marine environment represents an outstanding source of antitumoral compounds and,
at the same time, remains highly unexplored. Organisms living in the sea synthesize a wide …

[HTML][HTML] The 26S proteasome is a multifaceted target for anti-cancer therapies

TA Grigoreva, VG Tribulovich, AV Garabadzhiu… - Oncotarget, 2015 - ncbi.nlm.nih.gov
Proteasomes play a critical role in the fate of proteins that are involved in major cellular
processes, including signal transduction, gene expression, cell cycle, replication …

Matrine induces apoptosis in human acute myeloid leukemia cells via the mitochondrial pathway and Akt inactivation

S Zhang, Y Zhang, Y Zhuang, J Wang, J Ye, S Zhang… - 2012 - journals.plos.org
Acute myeloid leukemia (AML) is a hematological malignancy characterized by a rapid
increase in the number of immature myeloid cells in bone marrow. Despite recent advances …

Sorafenib enhances pemetrexed cytotoxicity through an autophagy-dependent mechanism in cancer cells

MD Bareford, MA Park, A Yacoub, HA Hamed, Y Tang… - Cancer research, 2011 - AACR
Pemetrexed (ALIMTA, Lilly) is a folate antimetabolite that has been approved by the US
Food and Drug Administration for the treatment of non–small cell lung cancer and has been …

[HTML][HTML] Functional exploration of colorectal cancer genomes using Drosophila

E Bangi, C Murgia, AGS Teague, OJ Sansom… - Nature …, 2016 - nature.com
The multigenic nature of human tumours presents a fundamental challenge for cancer drug
discovery. Here we use Drosophila to generate 32 multigenic models of colon cancer using …

The Bruton tyrosine kinase (BTK) inhibitor PCI‐32765 synergistically increases proteasome inhibitor activity in diffuse large‐B cell lymphoma (DLBCL) and mantle cell …

G Dasmahapatra, H Patel, P Dent… - British journal of …, 2013 - Wiley Online Library
Interactions between the Bruton tyrosine kinase (BTK) inhibitor PCI‐32765 and the
proteasome inhibitor (bortezomib) were examined in diffuse large‐B cell lymphoma …

Peptides, proteins and nanotechnology: A promising synergy for breast cancer targeting and treatment

A Sorolla, MA Sorolla, E Wang… - Expert opinion on drug …, 2020 - Taylor & Francis
Introduction The use of nanoparticles for breast cancer targeting and treatment has become
a reality. They are safe and possess interesting peculiarities such as the unspecific …

The role of angiogenesis in melanoma: Clinical treatments and future expectations

Z Wu, Y Bian, T Chu, Y Wang, S Man, Y Song… - Frontiers in …, 2022 - frontiersin.org
The incidence of melanoma has increased rapidly over the past few decades, with mortality
accounting for more than 75% of all skin cancers. The high metastatic potential of Melanoma …

[HTML][HTML] AURKA overexpression is driven by FOXM1 and MAPK/ERK activation in melanoma cells harboring BRAF or NRAS mutations: impact on melanoma …

JA Puig-Butille, A Vinyals, JR Ferreres… - Journal of Investigative …, 2017 - Elsevier
The cell cycle-related genes AURKA and FOXM1 are overexpressed in melanoma. We
show here that AURKA overexpression is associated with poor prognosis in three …

[HTML][HTML] PDGFRα up-regulation mediated by sonic hedgehog pathway activation leads to BRAF inhibitor resistance in melanoma cells with BRAF mutation

F Sabbatino, Y Wang, X Wang, KT Flaherty, L Yu… - Oncotarget, 2014 - ncbi.nlm.nih.gov
Abstract Control of BRAF (V600E) metastatic melanoma by BRAF inhibitor (BRAF-I) is
limited by intrinsic and acquired resistance. Growth factor receptor up-regulation is among …