Matches in SemOpenAlex for { <https://semopenalex.org/work/W2034170266> ?p ?o ?g. }
- W2034170266 endingPage "e23640" @default.
- W2034170266 startingPage "e23640" @default.
- W2034170266 abstract "Background Lnk plays a non-redundant role by negatively regulating cytokine signaling of TPO, SCF or EPO. Retroviral expression of Lnk has been shown to suppress hematopoietic leukemic cell proliferation indicating its therapeutic value in cancer therapy. However, retroviral gene delivery carries risks of insertional mutagenesis. To circumvent this undesired consequence, we fused a cell permeable peptide octa-arginine to Lnk and evaluated the efficacy of inhibition of leukemic cell proliferation in vitro. Methodology/Principal Findings In this study, proliferation assays, flow cytometry, Western Blot analyses were performed on wild-type (WT), mutant Lnk R8 or BSA treated M-MOK cells. We found that delivered WT, but not mutant Lnk R8 blocked TPO-induced M-MOK megakaryoblastic leukemic cell proliferation. In contrast, WT Lnk R8 showed no growth inhibitive effect on non-hematopoietic HELA or COS-7 cell. Moreover, we demonstrated that TPO-induced M-MOK cell growth inhibition by WT Lnk R8 was dose-dependent. Penetrated WT Lnk R8 induced cell cycle arrest and apoptosis. Immunoprecipitation and Western blots data indicated WT Lnk R8 interacted with endogeneous Jak2 and downregulated Jak-Stat and MAPK phosphorylation level in M-MOK cells after TPO stimulation. Treatment with specific inhibitors (TG101348 and PD98059) indicated Jak-Stat and MAPK pathways were crucial for TPO-induced proliferation of M-MOK cells. Further analyses using TF-1 and HEL leukemic cell-lines showed that WT Lnk R8 inhibited Jak2-dependent cell proliferation. Using cord blood-derived CD34+ stem cells, we found that delivered WT Lnk R8 blocked TPO-induced megakaryopoiesis in vitro. Conclusions/Significance Intracellular delivery of WT Lnk R8 fusion protein efficiently inhibited TPO-induced M-MOK leukemic cell growth by promoting apoptosis. WT Lnk R8 protein delivery may provide a safer and more practical approach to inhibit leukemic cell growth worthy of further development." @default.
- W2034170266 created "2016-06-24" @default.
- W2034170266 creator A5012086986 @default.
- W2034170266 creator A5012558697 @default.
- W2034170266 creator A5027375272 @default.
- W2034170266 creator A5027423432 @default.
- W2034170266 creator A5027642382 @default.
- W2034170266 creator A5040691390 @default.
- W2034170266 creator A5060303955 @default.
- W2034170266 creator A5075294352 @default.
- W2034170266 creator A5079155129 @default.
- W2034170266 date "2011-08-10" @default.
- W2034170266 modified "2023-10-18" @default.
- W2034170266 title "Octa-Arginine Mediated Delivery of Wild-Type Lnk Protein Inhibits TPO-Induced M-MOK Megakaryoblastic Leukemic Cell Growth by Promoting Apoptosis" @default.
- W2034170266 cites W1590937185 @default.
- W2034170266 cites W1641964996 @default.
- W2034170266 cites W1964904359 @default.
- W2034170266 cites W1979299941 @default.
- W2034170266 cites W1980568348 @default.
- W2034170266 cites W1981421312 @default.
- W2034170266 cites W1985506101 @default.
- W2034170266 cites W1995981641 @default.
- W2034170266 cites W2001215875 @default.
- W2034170266 cites W2009326620 @default.
- W2034170266 cites W2012262631 @default.
- W2034170266 cites W2022549031 @default.
- W2034170266 cites W2024621780 @default.
- W2034170266 cites W2029346749 @default.
- W2034170266 cites W2038818733 @default.
- W2034170266 cites W2049145190 @default.
- W2034170266 cites W2051345002 @default.
- W2034170266 cites W2055296721 @default.
- W2034170266 cites W2057879405 @default.
- W2034170266 cites W2065567658 @default.
- W2034170266 cites W2066778206 @default.
- W2034170266 cites W2069648201 @default.
- W2034170266 cites W2073726802 @default.
- W2034170266 cites W2075214128 @default.
- W2034170266 cites W2077426010 @default.
- W2034170266 cites W2082425467 @default.
- W2034170266 cites W2083289299 @default.
- W2034170266 cites W2084897544 @default.
- W2034170266 cites W2085577449 @default.
- W2034170266 cites W2088045605 @default.
- W2034170266 cites W2117494653 @default.
- W2034170266 cites W2118562509 @default.
- W2034170266 cites W2122263758 @default.
- W2034170266 cites W2123650819 @default.
- W2034170266 cites W2132012375 @default.
- W2034170266 cites W2132501668 @default.
- W2034170266 cites W2140619590 @default.
- W2034170266 cites W2144378152 @default.
- W2034170266 cites W2151115272 @default.
- W2034170266 cites W2152483372 @default.
- W2034170266 cites W2155819554 @default.
- W2034170266 cites W2161045200 @default.
- W2034170266 cites W2163176043 @default.
- W2034170266 cites W2165412794 @default.
- W2034170266 cites W2230842386 @default.
- W2034170266 cites W2253882122 @default.
- W2034170266 cites W2416937818 @default.
- W2034170266 cites W2423833205 @default.
- W2034170266 doi "https://doi.org/10.1371/journal.pone.0023640" @default.
- W2034170266 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3154509" @default.
- W2034170266 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/21853157" @default.
- W2034170266 hasPublicationYear "2011" @default.
- W2034170266 type Work @default.
- W2034170266 sameAs 2034170266 @default.
- W2034170266 citedByCount "28" @default.
- W2034170266 countsByYear W20341702662012 @default.
- W2034170266 countsByYear W20341702662013 @default.
- W2034170266 countsByYear W20341702662014 @default.
- W2034170266 countsByYear W20341702662015 @default.
- W2034170266 countsByYear W20341702662016 @default.
- W2034170266 countsByYear W20341702662017 @default.
- W2034170266 countsByYear W20341702662018 @default.
- W2034170266 countsByYear W20341702662021 @default.
- W2034170266 countsByYear W20341702662022 @default.
- W2034170266 crossrefType "journal-article" @default.
- W2034170266 hasAuthorship W2034170266A5012086986 @default.
- W2034170266 hasAuthorship W2034170266A5012558697 @default.
- W2034170266 hasAuthorship W2034170266A5027375272 @default.
- W2034170266 hasAuthorship W2034170266A5027423432 @default.
- W2034170266 hasAuthorship W2034170266A5027642382 @default.
- W2034170266 hasAuthorship W2034170266A5040691390 @default.
- W2034170266 hasAuthorship W2034170266A5060303955 @default.
- W2034170266 hasAuthorship W2034170266A5075294352 @default.
- W2034170266 hasAuthorship W2034170266A5079155129 @default.
- W2034170266 hasBestOaLocation W20341702661 @default.
- W2034170266 hasConcept C109159458 @default.
- W2034170266 hasConcept C153911025 @default.
- W2034170266 hasConcept C185592680 @default.
- W2034170266 hasConcept C190283241 @default.
- W2034170266 hasConcept C28328180 @default.
- W2034170266 hasConcept C29537977 @default.
- W2034170266 hasConcept C54355233 @default.
- W2034170266 hasConcept C553184892 @default.
- W2034170266 hasConcept C55493867 @default.