2023
DOI: 10.1016/j.biopha.2022.114162
|View full text |Cite
|
Sign up to set email alerts
|

Pharmacological targeting of the receptor ALK inhibits tumorigenicity and overcomes chemoresistance in pancreatic ductal adenocarcinoma

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2023
2023
2024
2024

Publication Types

Select...
5

Relationship

0
5

Authors

Journals

citations
Cited by 5 publications
(2 citation statements)
references
References 59 publications
(87 reference statements)
0
2
0
Order By: Relevance
“…RNAi-mediated abrogation of MDK restored the chemosensitivity of the resistant cells towards gemcitabine. Alonso et al blocked the ALK signaling pathway, which is one of the receptors for MDK binding, thereby inhibiting proliferation, self-renewal, tumorigenicity, and chemoresistance of the PDAC cells [26].…”
Section: Pancreatic Ductal Adenocarcinoma (Pdac)mentioning
confidence: 99%
See 1 more Smart Citation
“…RNAi-mediated abrogation of MDK restored the chemosensitivity of the resistant cells towards gemcitabine. Alonso et al blocked the ALK signaling pathway, which is one of the receptors for MDK binding, thereby inhibiting proliferation, self-renewal, tumorigenicity, and chemoresistance of the PDAC cells [26].…”
Section: Pancreatic Ductal Adenocarcinoma (Pdac)mentioning
confidence: 99%
“…Midkine is found to play a pivotal role in multi-drug resistance via different mechanisms such as inducing the overexpression of pro-proliferative molecules, inducing epithelial-mesenchymal transition (EMT), or others, such as increasing drug efflux pumps [22,24,25]. Inhibiting or downregulating MDK expression by using RNAi or siRNA shows drug sensitivity reverting to the resistant cells along with the enhancement in the efficacy of the chemotherapeutic agent [26,27]. However, not much is known about the regulation of MDK's expression and function.…”
Section: Introductionmentioning
confidence: 99%