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Role of c-Abl in the DNA damage stress response

https://doi.org/10.1038/sj.cr.7290261
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1016/s0092-8674(02)00623-2openalex-snapshot
Autoinhibition of c-Abl
inferredcites →https://doi.org/10.1016/s0304-419x(97)00020-6openalex-snapshot
Functional role for the c-Abl protein tyrosine kinase in the cellular response to genotoxic stress
inferredcites →https://doi.org/10.1038/21539openalex-snapshot
DNA damage enables p73
inferredcites →https://doi.org/10.1038/21697openalex-snapshot
Interaction of c-Abl and p73α and their collaboration to induce apoptosis
inferredcites →https://doi.org/10.1038/ncb0104-3openalex-snapshot
Controlling Abl: auto-inhibition and co-inhibition?
inferredcites →https://doi.org/10.1038/nrc1011openalex-snapshot
ATM and related protein kinases: safeguarding genome integrity
inferredcites →https://doi.org/10.1038/sj.cdd.4400626openalex-snapshot
c-Abl: activation and nuclear targets
inferredcites →https://doi.org/10.1073/pnas.95.13.7457openalex-snapshot
Nuclear-cytoplasmic shuttling of C-ABL tyrosine kinase
inferredcites →https://doi.org/10.1074/jbc.m301051200openalex-snapshot
c-Abl Tyrosine Kinase Selectively Regulates p73 Nuclear Matrix Association

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4781335openalex-extracted
The Abl1 Tyrosine Kinase and p53 are Key Players in Doxorubicin-Induced Cardiomyopathy and Their Cell Death Signaling Differs in Atrial and Ventricular Cardiomyocytes
inferred← citeshttps://doi.org/10.1002/cbin.10413openalex-snapshot
c‐Abl induces stabilization of histone deacetylase 1 (HDAC1) in a kinase activity‐dependent manner
inferred← citeshttps://doi.org/10.1002/eji.200737221openalex-snapshot
c‐Abl is required for the signaling transduction induced by L‐selectin ligation
inferred← citeshttps://doi.org/10.1002/mc.20721openalex-snapshot
Overcoming resistance to fulvestrant (ICI182,780) by Downregulating the c‐ABL Proto‐Oncogene in breast cancer
inferred← citeshttps://doi.org/10.1002/mrd.70039openalex-snapshot
c‐Abl Plays an Important Role in Mouse Preimplantation Embryo Development and the Dysregulation Associated With Decreased mTERT Expression
inferred← citeshttps://doi.org/10.1007/978-1-4614-6220-0_9openalex-snapshot
The c-Abl/YAP/p73 Apoptotic Module and the HIPPO Pathway
inferred← citeshttps://doi.org/10.1007/s00216-026-06333-4openalex-snapshot
DNA sandwich nanozyme-based colorimetric and photothermal biosensor for high-efficiency detection of fusion genes
inferred← citeshttps://doi.org/10.1007/s00441-011-1146-1openalex-snapshot
Protein tyrosine phosphatase interacting protein 51—a jack-of-all-trades protein
inferred← citeshttps://doi.org/10.1007/s10237-019-01224-3openalex-snapshot
Cyclic stretch-induced mechanical stress to the cell nucleus inhibits ultraviolet radiation-induced DNA damage
inferred← citeshttps://doi.org/10.1007/s10495-008-0285-7openalex-snapshot
Involvement of c-Abl, p53 and the MAP kinase JNK in the cell death program initiated in A2E-laden ARPE-19 cells by exposure to blue light
inferred← citeshttps://doi.org/10.1007/s10565-012-9232-zopenalex-snapshot
Dynamic changes in nuclear localization of a DNA-binding protein tyrosine phosphatase TCPTP in response to DNA damage and replication arrest
inferred← citeshttps://doi.org/10.1007/s10735-011-9310-1openalex-snapshot
The abelson tyrosine kinase (c-Abl) expression on the mouse uterus and placenta during gestational period
inferred← citeshttps://doi.org/10.1007/s11011-025-01664-0openalex-snapshot
Exploration of Imatinib involved in amyloidogenesis as a common foundation for type-2 diabetes mellitus (T2DM) and Alzheimer’s disease (AD)
inferred← citeshttps://doi.org/10.1007/s13353-018-0432-yopenalex-snapshot
Tip60: updates
inferred← citeshttps://doi.org/10.1016/b978-0-12-374984-0.00185-6openalex-snapshot
c-ABL Gene and Gene Product
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2018.05.014openalex-snapshot
c-Abl phosphorylation of Yin Yang 1's conserved tyrosine 254 in the spacer region modulates its transcriptional activity
inferred← citeshttps://doi.org/10.1016/j.bcp.2011.07.001openalex-snapshot
DNA damage response: The emerging role of c-Abl as a regulatory switch?
inferred← citeshttps://doi.org/10.1016/j.cellsig.2013.10.005openalex-snapshot
c-ABL tyrosine kinase modulates p53-dependent p21 induction and ensuing cell fate decision in response to DNA damage
inferred← citeshttps://doi.org/10.1016/j.clon.2005.11.011openalex-snapshot
Radiobiology of Breast Cancer
inferred← citeshttps://doi.org/10.1016/j.febslet.2006.03.089openalex-snapshot
Protein kinase PKC delta and c‐Abl are required for mitochondrial apoptosis induction by genotoxic stress in the absence of p53, p73 and Fas receptor
inferred← citeshttps://doi.org/10.1016/j.humimm.2008.06.005openalex-snapshot
L-selectin ligation-induced CSF-1 gene transcription is regulated by AP-1 in a c-Abl kinase-dependent manner
inferred← citeshttps://doi.org/10.1016/j.jbc.2021.100883openalex-snapshot
Platelet-derived growth factor receptor beta activates Abl2 via direct binding and phosphorylation
inferred← citeshttps://doi.org/10.1016/j.molcel.2007.12.022openalex-snapshot
Yap1 Phosphorylation by c-Abl Is a Critical Step in Selective Activation of Proapoptotic Genes in Response to DNA Damage
inferred← citeshttps://doi.org/10.1016/j.molliq.2016.08.064openalex-snapshot
Anticancer effects of silver nanoparticles encapsulated by Taxus baccata extracts
inferred← citeshttps://doi.org/10.1016/j.neo.2018.09.002openalex-snapshot
Interaction of Abl Tyrosine Kinases with SOCS3 Impairs Its Suppressor Function in Tumorigenesis
inferred← citeshttps://doi.org/10.1016/j.pharmr.2026.100128openalex-snapshot
Targeting of kinases to treat neurodegenerative diseases
inferred← citeshttps://doi.org/10.1016/j.prp.2024.155161openalex-snapshot
The impact of the BCR-ABL oncogene in the pathology and treatment of chronic myeloid leukemia
inferred← citeshttps://doi.org/10.1016/j.repbio.2020.10.004openalex-snapshot
Determination of c-Abl tyrosine kinase and mTERT catalytic subunit of telomerase expression level during prenatal-postnatal mouse ovary-testis development
inferred← citeshttps://doi.org/10.1016/j.reprotox.2009.01.014openalex-snapshot
Teratogen responsive signaling pathways in organogenesis stage mouse limbs
inferred← citeshttps://doi.org/10.1016/j.yexcr.2011.09.013openalex-snapshot
Nuclear c-Abl-mediated tyrosine phosphorylation induces chromatin structural changes through histone modifications that include H4K16 hypoacetylation
inferred← citeshttps://doi.org/10.1016/j.yexcr.2013.09.003openalex-snapshot
Formation of long and winding nuclear F-actin bundles by nuclear c-Abl tyrosine kinase
inferred← citeshttps://doi.org/10.1021/bi301710copenalex-snapshot
c-Abl Phosphorylates E6AP and Regulates Its E3 Ubiquitin Ligase Activity
inferred← citeshttps://doi.org/10.1021/jacs.0c06599openalex-snapshot
Ultrasensitive Detection of Enzymatic Activity Using Single Molecule Arrays
inferred← citeshttps://doi.org/10.1038/cdd.2010.132openalex-snapshot
c-Abl tyrosine kinase in the DNA damage response: cell death and more
inferred← citeshttps://doi.org/10.1038/cddis.2009.15openalex-snapshot
c-Abl phosphorylation of ΔNp63α is critical for cell viability
inferred← citeshttps://doi.org/10.1038/cddis.2009.21openalex-snapshot
c-Abl downregulates the slow phase of double-strand break repair
inferred← citeshttps://doi.org/10.1038/nrc3563openalex-snapshot
Role of ABL family kinases in cancer: from leukaemia to solid tumours
inferred← citeshttps://doi.org/10.1038/onc.2008.68openalex-snapshot
Pharmacological inhibition of c-Abl compromises genetic stability and DNA repair in Bcr-Abl-negative cells
inferred← citeshttps://doi.org/10.1038/onc.2010.410openalex-snapshot
DNA damage stress response in germ cells: role of c-Abl and clinical implications
inferred← citeshttps://doi.org/10.1038/onc.2013.84openalex-snapshot
The Ron receptor tyrosine kinase activates c-Abl to promote cell proliferation through tyrosine phosphorylation of PCNA in breast cancer
inferred← citeshttps://doi.org/10.1038/s41418-024-01339-wopenalex-snapshot
ABL1-mediated phosphorylation promotes FOXM1-related tumorigenicity by Increasing FOXM1 stability
inferred← citeshttps://doi.org/10.1038/s41467-020-17770-9openalex-snapshot
ABL1-dependent OTULIN phosphorylation promotes genotoxic Wnt/β-catenin activation to enhance drug resistance in breast cancers
inferred← citeshttps://doi.org/10.1038/s44319-025-00613-3openalex-snapshot
Loss of the lysosomal protein CLN3 triggers c-Abl-dependent YAP1 pro-apoptotic signaling
inferred← citeshttps://doi.org/10.1038/sj.onc.1209671openalex-snapshot
c-Abl phosphorylates Hdm2 at tyrosine 276 in response to DNA damage and regulates interaction with ARF
inferred← citeshttps://doi.org/10.1038/srep24504openalex-snapshot
The dynamic behavior of Ect2 in response to DNA damage
inferred← citeshttps://doi.org/10.1042/bj20150372openalex-snapshot
c-Abl-mediated tyrosine phosphorylation of JunB is required for Adriamycin-induced expression of p21
inferred← citeshttps://doi.org/10.1074/jbc.m117.803338openalex-snapshot
Nuclear Gene 33/Mig6 regulates the DNA damage response through an ATM serine/threonine kinase–dependent mechanism
inferred← citeshttps://doi.org/10.1074/jbc.m803941200openalex-snapshot
A Regulatory Circuit Controlling Itch-mediated p73 Degradation by Runx
inferred← citeshttps://doi.org/10.1074/jbc.m804002200openalex-snapshot
Enhancement of ABL Kinase Catalytic Efficiency by a Direct Binding Regulator Is Independent of Other Regulatory Mechanisms
inferred← citeshttps://doi.org/10.1074/jbc.m809211200openalex-snapshot
c-Abl Phosphorylates Hdmx and Regulates Its Interaction with p53
inferred← citeshttps://doi.org/10.1080/01902148.2020.1836691openalex-snapshot
Ponatinib is a potential therapeutic approach for malignant pleural mesothelioma
inferred← citeshttps://doi.org/10.1080/07357900701600954openalex-snapshot
Downregulation of Survivin Is Associated With Reductions in TNF Receptors' mRNA and Protein and Alterations in Nuclear Factor Kappa B Signaling in Urothelial Cancer Cells
inferred← citeshttps://doi.org/10.1080/10799893.2020.1735419openalex-snapshot
Interaction of the mTERT telomerase catalytic subunit with the c-Abl tyrosine kinase in mouse granulosa cells
inferred← citeshttps://doi.org/10.1091/mbc.e18-02-0130openalex-snapshot
Extracellular vesicles transfer nuclear Abl-dependent and radiation-induced miR-34c into unirradiated cells to cause bystander effects
inferred← citeshttps://doi.org/10.1093/humupd/dms022openalex-snapshot
How do chemotherapeutic agents damage the ovary?
inferred← citeshttps://doi.org/10.1093/narcan/zcaf031openalex-snapshot
ABL1-mediated tyrosine phosphorylation of SYCP2 contributes to transcription-coupled homologous recombination and platinum resistance in ovarian cancer
inferred← citeshttps://doi.org/10.1101/2025.03.27.645704openalex-snapshot
c-Abl Phosphorylates Plk1 in Facilitating DNA Damage-Induced G2/M Checkpoint Release with a Trade-off of Micronuclei Formation
inferred← citeshttps://doi.org/10.1101/209767openalex-snapshot
Nuclear Abl Drives miR-34c Transfer by Extracellular Vesicles to Induce Radiation Bystander Effects
inferred← citeshttps://doi.org/10.1111/andr.12803openalex-snapshot
Association of hMSH5 C85T polymorphism with radiation sensitivity of testicular cell lines GC‐1, GC‐2, TM3, and TM4
inferred← citeshttps://doi.org/10.1126/scisignal.3139re6openalex-snapshot
ABL Tyrosine Kinases: Evolution of Function, Regulation, and Specificity
inferred← citeshttps://doi.org/10.1128/mcb.01454-13openalex-snapshot
The Capable ABL: What Is Its Biological Function?
inferred← citeshttps://doi.org/10.1158/0008-5472.can-16-1378openalex-snapshot
Cervical Cancer Growth Is Regulated by a c-ABL–PLK1 Signaling Axis
inferred← citeshttps://doi.org/10.1165/rcmb.2021-0332ocopenalex-snapshot
Loss of cAbl Tyrosine Kinase in Pulmonary Arterial Hypertension Causes Dysfunction of Vascular Endothelial Cells
inferred← citeshttps://doi.org/10.1182/blood-2011-07-367557openalex-snapshot
RNAi screening of the kinome with cytarabine in leukemias
inferred← citeshttps://doi.org/10.1182/blood.2023021225openalex-snapshot
ABL1 kinase plays an important role in spontaneous and chemotherapy-induced genomic instability in multiple myeloma
inferred← citeshttps://doi.org/10.1186/1476-4598-10-88openalex-snapshot
Tip60-mediated acetylation activates transcription independent apoptotic activity of Abl
inferred← citeshttps://doi.org/10.1186/2041-9414-3-2openalex-snapshot
Differential regulation of intracellular factors mediating cell cycle, DNA repair and inflammation following exposure to silver nanoparticles in human cells
inferred← citeshttps://doi.org/10.1186/s12867-016-0065-9openalex-snapshot
A potential role for protein palmitoylation and zDHHC16 in DNA damage response
inferred← citeshttps://doi.org/10.1186/s12885-025-14764-yopenalex-snapshot
Inhibition of c-Abl suppresses the proliferation, invasion and migration of glioma cells
inferred← citeshttps://doi.org/10.1186/s12943-018-0792-2openalex-snapshot
Receptor tyrosine kinases and downstream pathways as druggable targets for cancer treatment: the current arsenal of inhibitors
inferred← citeshttps://doi.org/10.1186/s12964-019-0323-9openalex-snapshot
Helicobacter pylori-controlled c-Abl localization promotes cell migration and limits apoptosis
inferred← citeshttps://doi.org/10.1186/s12967-024-05623-8openalex-snapshot
The Abl1 tyrosine kinase is a key player in doxorubicin-induced cardiomyopathy and its p53/p73 cell death mediated signaling differs in atrial and ventricular cardiomyocytes
inferred← citeshttps://doi.org/10.1186/s13046-016-0414-zopenalex-snapshot
Inhibition of YAP suppresses CML cell proliferation and enhances efficacy of imatinib in vitro and in vivo
inferred← citeshttps://doi.org/10.1371/journal.pone.0095663openalex-snapshot
Geminin Overexpression Promotes Imatinib Sensitive Breast Cancer: A Novel Treatment Approach for Aggressive Breast Cancers, Including a Subset of Triple Negative
inferred← citeshttps://doi.org/10.1371/journal.pone.0100950openalex-snapshot
Reduced Expression of the Retinoblastoma Protein Shows That the Related Signaling Pathway Is Essential for Mediating the Antineoplastic Activity of Erufosine
inferred← citeshttps://doi.org/10.15407/ubj85.01.051openalex-snapshot
Biochemical effects of combined action of ?-irradiation and paclitaxel on anaplastic thyroid cancer cells
inferred← citeshttps://doi.org/10.1593/neo.91576openalex-snapshot
Enhanced Resistance to Tamoxifen by the c-ABL Proto-oncogene in Breast Cancer
inferred← citeshttps://doi.org/10.21203/rs.2.12071/v2openalex-snapshot
Regulation of the mTERT telomerase catalytic subunit by the c-Abl tyrosine kinase in mouse granulosa cells
inferred← citeshttps://doi.org/10.2147/cmar.s373557openalex-snapshot
Genotoxicity-Stimulated and CYLD-Driven Malignant Transformation
inferred← citeshttps://doi.org/10.2353/jmoldx.2006.040404openalex-snapshot
Molecular Monitoring of Chronic Myelogenous Leukemia
inferred← citeshttps://doi.org/10.2353/jmoldx.2006.050150openalex-snapshot
β-Glucuronidase Is an Optimal Normalization Control Gene for Molecular Monitoring of Chronic Myelogenous Leukemia
inferred← citeshttps://doi.org/10.32725/jab.2006.009openalex-snapshot
Imatinib mesylate affects tyrosine kinase activity in both leukemic and normal primary mononuclear blood cells
inferred← citeshttps://doi.org/10.3389/fcell.2022.844297openalex-snapshot
c-Abl Activation Linked to Autophagy-Lysosomal Dysfunction Contributes to Neurological Impairment in Niemann-Pick Type A Disease
inferred← citeshttps://doi.org/10.3390/cells10071574openalex-snapshot
Gene 33/Mig6/ERRFI1, an Adapter Protein with Complex Functions in Cell Biology and Human Diseases
inferred← citeshttps://doi.org/10.3390/cells14181461openalex-snapshot
NUP214 in Acute Myeloid Leukemia
inferred← citeshttps://doi.org/10.3390/ijms14022388openalex-snapshot
Parkinson’s Disease: A Complex Interplay of Mitochondrial DNA Alterations and Oxidative Stress
inferred← citeshttps://doi.org/10.3390/toxins11100591openalex-snapshot
Tyrosine Kinases in Helicobacter pylori Infections and Gastric Cancer
inferred← citeshttps://doi.org/10.3892/mmr.2020.11156openalex-snapshot
c‑Abl‑mediated tyrosine phosphorylation of DNA damage response proteins and implications in important cellular functions (Review)
inferred← citeshttps://doi.org/10.3892/ol.2016.4637openalex-snapshot
Identification of disease-associated pathways in pancreatic cancer by integrating genome-wide association study and gene expression data
inferred← citeshttps://doi.org/10.3892/or.2013.2829openalex-snapshot
Decreased c-Abl activity in PC-3 and LNCaP prostate cancer cells overexpressing the early growth response-1 protein
inferred← citeshttps://doi.org/10.4149/neo_2019_190131n94openalex-snapshot
Second-generation Src/Abl inhibitor bosutinib effectively induces apoptosis in human esophageal squamous cell carcinoma (ESCC) cells via inhibiting Src/Abl signaling
inferred← citeshttps://doi.org/10.4161/cc.7.24.7267openalex-snapshot
T cell survival and function requires the c-Abl tyrosine kinase
inferred← citeshttps://doi.org/10.70675/5c76ff65ze75ez4b18z8a86zb49fcf8bbecdopenalex-snapshot
Etude structurale et fonctionnelle d'un domaine intrinsèquement désordonné de l'oncoprotéine BCR-ABL responsable de la leucémie myéloïde chronique
inferred← citeshttps://doi.org/10.70675/75a0e54fz1904z486bz8ca5z986ca9a01f62openalex-snapshot
Etude de la régulation et des fonctions d'ArgBP2 associées à son rôle anti-tumoral et aux processus dépendants de l'actine : rôle de ses partenaires moléculaires, de sa phosphorylation et de sa dimérisation
inferred← citeshttps://doi.org/10.7150/jca.47318openalex-snapshot
Co-overexpression of AXL and c-ABL predicts a poor prognosis in esophageal adenocarcinoma and promotes cancer cell survival
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