ATP-binding cassette efflux transporters and MDR in cancer
MS Pote, RN Gacche - Drug Discovery Today, 2023 - Elsevier
Highlights•The most common reason for the failure of the cancer treatment is the evolving
drug resistance.•The ABC transporters mainly P-gp, BCRP and MRP1 are responsible for …
drug resistance.•The ABC transporters mainly P-gp, BCRP and MRP1 are responsible for …
[HTML][HTML] Functional roles of JNK and p38 MAPK signaling in nasopharyngeal carcinoma
c-Jun N-terminal kinase (JNK) and p38 mitogen-activated protein kinase (MAPK) family
members integrate signals that affect proliferation, differentiation, survival, and migration in a …
members integrate signals that affect proliferation, differentiation, survival, and migration in a …
JNK signaling in cancer cell survival
Q Wu, W Wu, B Fu, L Shi, X Wang… - Medicinal research …, 2019 - Wiley Online Library
Abstract c‐Jun N‐terminal kinase (JNK) is involved in cancer cell apoptosis; however,
emerging evidence indicates that this Janus signaling promotes cancer cell survival. JNK …
emerging evidence indicates that this Janus signaling promotes cancer cell survival. JNK …
[HTML][HTML] Mechanisms of drug resistance in colon cancer and its therapeutic strategies
Drug resistance develops in nearly all patients with colon cancer, leading to a decrease in
the therapeutic efficacies of anticancer agents. This review provides an up-to-date summary …
the therapeutic efficacies of anticancer agents. This review provides an up-to-date summary …
Multidrug efflux transporter ABCG2: expression and regulation
The adenosine triphosphate (ATP)-binding cassette efflux transporter G2 (ABCG2) was
originally discovered in a multidrug-resistant breast cancer cell line. Studies in the past have …
originally discovered in a multidrug-resistant breast cancer cell line. Studies in the past have …
Targeting breast cancer resistance protein (BCRP/ABCG2): Functional inhibitors and expression modulators
IF Zattoni, LC Delabio, J de Paula Dutra, DH Kita… - European journal of …, 2022 - Elsevier
The primary source of failure of cancer therapies is multidrug resistance (MDR), which can
be caused by different mechanisms, including the overexpression of ABC transporters in …
be caused by different mechanisms, including the overexpression of ABC transporters in …
[HTML][HTML] Dysregulated signalling pathways driving anticancer drug resistance
N Bou Antoun, AM Chioni - International journal of molecular sciences, 2023 - mdpi.com
One of the leading causes of death worldwide, in both men and women, is cancer. Despite
the significant development in therapeutic strategies, the inevitable emergence of drug …
the significant development in therapeutic strategies, the inevitable emergence of drug …
Unraveling the journey of cancer stem cells from origin to metastasis
Cancer biology research over recent decades has given ample evidence for the existence of
self-renewing and drug-resistant populations within heterogeneous tumors, widely …
self-renewing and drug-resistant populations within heterogeneous tumors, widely …
The upregulation of PI3K/Akt and MAP kinase pathways is associated with resistance of microtubule‐targeting drugs in prostate cancer
Z Liu, G Zhu, RH Getzenberg… - Journal of cellular …, 2015 - Wiley Online Library
Resistance is a significant limitation to the effectiveness of cancer therapies. The PI3K/Akt
and MAP kinase pathways play important roles in a variety of normal cellular processes and …
and MAP kinase pathways play important roles in a variety of normal cellular processes and …
The ellagic acid-derived gut microbiota metabolite, urolithin A, potentiates the anticancer effects of 5-fluorouracil chemotherapy on human colon cancer cells
A González-Sarrías, J Tomé-Carneiro, A Bellesia… - Food & function, 2015 - pubs.rsc.org
Chemotherapy increases the overall survival in colorectal cancer (CRC) patients. 5-
Fluorouracil (5-FU) remains as a drug of first choice in CRC therapy over the last four …
Fluorouracil (5-FU) remains as a drug of first choice in CRC therapy over the last four …