Mechanisms of multidrug resistance in cancer chemotherapy

K Bukowski, M Kciuk, R Kontek - International journal of molecular …, 2020 - mdpi.com
Cancer is one of the main causes of death worldwide. Despite the significant development of
methods of cancer healing during the past decades, chemotherapy still remains the main …

DNA damage/repair management in cancers

JF Alhmoud, JF Woolley… - Advances in Medical …, 2021 - api.taylorfrancis.com
DNA damage can alter nucleotide sequences and lead to expression of dysfunctional
proteins that impact normal cellular physiology. Sources of DNA damage can be …

DNA repair pathways and cisplatin resistance: an intimate relationship

CRR Rocha, MM Silva, A Quinet, JB Cabral-Neto… - Clinics, 2018 - SciELO Brasil
The main goal of chemotherapeutic drugs is to induce massive cell death in tumors.
Cisplatin is an antitumor drug widely used to treat several types of cancer. Despite its …

A nuclease-mimetic platinum nanozyme induces concurrent DNA platination and oxidative cleavage to overcome cancer drug resistance

F Li, H Sun, J Ren, B Zhang, X Hu, C Fang… - Nature …, 2022 - nature.com
Platinum (Pt) resistance in cancer almost inevitably occurs during clinical Pt-based
chemotherapy. The spontaneous nucleotide-excision repair of cancer cells is a …

[HTML][HTML] Revisiting the hallmarks of cancer

YA Fouad, C Aanei - American journal of cancer research, 2017 - ncbi.nlm.nih.gov
The hallmarks of cancer described by Hanahan and Weinberg have proved seminal in our
understanding of cancer's common traits and in rational drug design. Not free of critique and …

Drugging the cancers addicted to DNA repair

JA Nickoloff, D Jones, SH Lee… - JNCI: Journal of the …, 2017 - academic.oup.com
Defects in DNA repair can result in oncogenic genomic instability. Cancers occurring from
DNA repair defects were once thought to be limited to rare inherited mutations (such as …

Discovery of first-in-class dual PARP and EZH2 inhibitors for triple-negative breast cancer with wild-type BRCA

C Wang, L Qu, S Li, F Yin, L Ji, W Peng… - Journal of Medicinal …, 2021 - ACS Publications
PARP inhibitors have highly significant effects on BRCA mutant cells, allowing targeted
therapy of triple-negative breast cancer (TNBC). However, some TBNC patients lack BRCA …

Exploiting the Ref-1-APE1 node in cancer signaling and other diseases: from bench to clinic

F Shah, D Logsdon, RA Messmann… - NPJ precision …, 2017 - nature.com
Abstract Reduction-oxidation factor 1-apurinic/apyrimidinic endonuclease (Ref-1/APE1) is a
critical node in tumor cells, both as a redox regulator of transcription factor activation and as …

The human AP-endonuclease 1 (APE1) is a DNA G-quadruplex structure binding protein and regulates KRAS expression in pancreatic ductal adenocarcinoma cells

S Pramanik, Y Chen, H Song, I Khutsishvili… - Nucleic acids …, 2022 - academic.oup.com
Pancreatic ductal adenocarcinoma (PDAC), one of the most aggressive types of cancer, is
characterized by aberrant activity of oncogenic KRAS. A nuclease-hypersensitive GC-rich …

Carbonic anhydrase IX inhibitors as candidates for combination therapy of solid tumors

S Kalinin, A Malkova, T Sharonova, V Sharoyko… - International Journal of …, 2021 - mdpi.com
Combination therapy is becoming imperative for the treatment of many cancers, as it
provides a higher chance of avoiding drug resistance and tumor recurrence. Among the …