Differential sensitivity of breast cancer and melanoma cells to proteasome inhibitor Velcade

A Yerlikaya, N Erin - International journal of molecular …, 2008 - spandidos-publications.com
Velcade (also known as PS-341 or Bortezomib) is a highly selective and reversible inhibitor
of the 26S proteasome and is approved for the treatment of patients with advanced multiple …

New trends in synthetic drugs and natural products targeting 20S proteasomes in cancers

H Atta, N Alzahaby, NM Hamdy, SH Emam… - Bioorganic …, 2023 - Elsevier
Cancer is a global health challenge that remains to be a field of extensive research aiming
to find new anticancer therapeutics. The 20S proteasome complex is one of the targets of …

Treating MCF7 breast cancer cell with proteasome inhibitor Bortezomib restores apoptotic factors and sensitizes cell to Docetaxel

K Mehdizadeh, F Ataei, S Hosseinkhani - Medical Oncology, 2021 - Springer
Chemoresistance is the leading cause of limiting long-term treatment success in cancer
cells. Anticancer drugs usually kill cells through apoptosis induction and defects in this …

Discovery of a novel dipeptidyl boronic acid proteasome inhibitor for the treatment of multiple myeloma and triple-negative breast cancer

M Lei, H Feng, E Bai, H Zhou, J Wang, Y Qin… - Organic & …, 2019 - pubs.rsc.org
A series of novel dipeptidyl boronic acid compounds were designed, synthesized and
biologically investigated for the inhibition of the β5 subunit of 20S proteasome and several …

A novel combination treatment for breast cancer cells involving BAPTA-AM and proteasome inhibitor bortezomib

A Yerlikaya, E Erdoğan, E Okur… - Oncology …, 2016 - spandidos-publications.com
Glucose-regulated protein 78 kDa/binding immunoglobulin protein (GRP78/BIP) is a well-
known endoplasmic reticulum (ER) chaperone protein regulating ER stress by facilitating …

Effect of bortezomib in combination with cisplatin and 5‑fluorouracil on 4T1 breast cancer cells

A Yerlikaya, S Altıkat, R Irmak… - Molecular …, 2013 - spandidos-publications.com
Bortezomib is a highly selective and reversible inhibitor of the 26S proteasome. It has been
approved for the treatment of patients with relapsed and refractory multiple myeloma. A …

Changes in proteasome pool in human papillary thyroid carcinoma development

N Sharova, T Astakhova, Y Karpova, Y Lyupina… - Open life …, 2011 - degruyter.com
Searching the antitumor drug targets among proteasomes,“ubiquitous” enzyme systems,
may provide a new impulse to the antitumor drug discovery. In this study, changes in the …

Diminished feedback regulation of proteasome expression and resistance to proteasome inhibitors in breast cancer cells

H Xu, D Ju, T Jarois, Y Xie - Breast cancer research and treatment, 2008 - Springer
Clinical trials with proteasome inhibitor Bortezomib (also named Velcade or PS-341) has
shown promising results for some cancers. However, other types of cancers including breast …

[HTML][HTML] Biodistribution and efficacy studies of the proteasome inhibitor BSc2118 in a mouse melanoma model

I Mlynarczuk-Bialy, TR Doeppner, J Golab, D Nowis… - Translational …, 2014 - Elsevier
Inhibition of the proteasome offers many therapeutic possibilities in inflammation as well as
in neoplastic diseases. However, clinical use of proteasome inhibitors is limited by the …

[HTML][HTML] Prognostic and immune infiltration signatures of proteasome 26S subunit, non-ATPase (PSMD) family genes in breast cancer patients

CC Wu, TJ Kao, HDK Ta, G Anuraga, V Andriani… - Aging (albany …, 2021 - ncbi.nlm.nih.gov
The complexity of breast cancer includes many interacting biological processes that make it
difficult to find appropriate therapeutic treatments. Therefore, identifying potential diagnostic …