| 1998 |
TIP30 (HTATIP2) interacts with HIV-1 Tat and with an SRB-containing RNA polymerase II complex both in vivo and in vitro; immunodepletion of TIP30 from nuclear extracts abolishes Tat-activated transcription without affecting Tat-independent transcription, establishing TIP30 as a specific coactivator for Tat-dependent transcription elongation. |
Co-immunoprecipitation (in vivo and in vitro), immunodepletion from nuclear extracts, transfection-based transcription assay |
Proceedings of the National Academy of Sciences of the United States of America |
High |
9482853
|
| 2000 |
TIP30/CC3 possesses intrinsic serine/threonine kinase activity; it phosphorylates the heptapeptide repeats of the C-terminal domain (CTD) of the largest RNA polymerase II subunit in a Tat-dependent manner. Amino acid substitutions in the putative ATP-binding motif that abolish kinase activity also abolish TIP30's ability to enhance Tat-activated transcription and to sensitize cells to apoptosis. Ectopic TIP30 induces expression of apoptosis-related genes Bad and Siva and metastasis suppressor NM23-H2. |
In vitro kinase assay, active-site mutagenesis, transfection-based transcription assay, gene expression profiling |
The EMBO journal |
High |
10698937
|
| 2000 |
CC3/TIP30 predisposes cells to apoptosis by disrupting mitochondrial membrane potential (ΔΨm). An alternatively spliced product, TC3, which shares the N-terminal domain of CC3 but has a unique hydrophobic C-terminus, has opposing antiapoptotic activity and forms complexes with the s5α regulatory subunit of the proteasome; TC3 is rapidly degraded by the proteasome. The proapoptotic activity of CC3 resides in its N-terminal domain. |
Overexpression, deletion/mutagenesis of CC3/TC3, cell death assay, mitochondrial membrane potential measurement, co-immunoprecipitation with proteasome subunit, proteasome inhibitor experiments |
Molecular and cellular biology |
High |
10611237
|
| 2001 |
Expression of CC3/TIP30 in tumor cell lines significantly reduces their angiogenic properties, as measured by inhibition of endothelial cell proliferation and migration in vitro, and alters RNA levels of several angiogenic modulators. |
Overexpression in tumor cell lines, in vitro endothelial cell proliferation and migration assays, RNA expression analysis |
Oncogene |
Medium |
11313954
|
| 2003 |
TIP30-deficient (Tip30−/−) mice develop hepatocellular carcinoma and other tumors at higher incidence than wild-type mice, establishing Tip30 as an in vivo tumor susceptibility gene. Loss of TIP30 also enhances susceptibility of fibroblasts to transformation by SV40 large T antigen. |
Genetically engineered knockout mice, tumor incidence analysis, fibroblast transformation assay |
Cancer research |
High |
14695192
|
| 2004 |
CC3/TIP30 directly binds karyopherins of the importin beta family in a RanGTP-insensitive manner and associates with nucleoporins in vivo. This interaction inhibits nuclear import of proteins bearing classical NLS or M9 signals. A CC3 mutant lacking proapoptotic activity shows lower affinity for transportin, is displaced by RanGTP, and fails to inhibit nuclear import. Inhibition of nuclear import correlates with proapoptotic activity. |
In vitro nuclear import assay, in vivo nuclear import assay, direct binding assay (pulldown), mutagenesis, RanGTP competition assay |
Molecular and cellular biology |
High |
15282309
|
| 2004 |
TIP30 interacts with ERα-interacting coactivator CIA; both are dynamically recruited to the c-myc gene promoter and downstream regions in response to estrogen, as shown by chromatin immunoprecipitation. TIP30 overexpression represses ERα-mediated c-myc transcription, while TIP30 deficiency enhances c-myc transcription. Ectopic CIA cooperates with TIP30 to repress ERα-mediated c-myc transcription. |
Co-immunoprecipitation, chromatin immunoprecipitation (ChIP), overexpression/knockout cell assays, TIP30 knockout mouse mammary gland analysis |
The Journal of biological chemistry |
High |
15073177
|
| 2005 |
Crystal structure of CC3/TIP30 at 1.7-Å resolution reveals a short-chain dehydrogenase/reductase (SDR) fold with binding specificity for NADPH. The protein is monomeric and unlikely to be enzymatically active in the canonical SDR sense. Structural analysis, in conjunction with prior mutagenesis data, suggests NADPH binding is important for biological activity including interaction with importins and the CIA/c-myc system. |
X-ray crystallography (1.7 Å resolution), structural analysis, NADPH binding |
The Journal of biological chemistry |
High |
15728189
|
| 2007 |
TIP30 mutants derived from HCC specimens promote cell growth and invasion while inhibiting cisplatin-induced apoptosis in HepG2 cells negative for endogenous TIP30. One mutant dramatically accelerates tumor formation in immunodeficient mice. Mutant TIP30 upregulates N-cadherin and c-MYC and downregulates p53 and E-cadherin; N-cadherin knockdown in mutant-expressing cells causes profound reduction in cell viability. |
Overexpression of mutant TIP30, Affymetrix GeneChip array, real-time PCR, Western blotting, siRNA knockdown of N-cadherin, in vivo xenograft |
Cancer research |
Medium |
17440068
|
| 2008 |
TIP30 regulates p53 mRNA stability under oxidative stress. Under oxidative conditions, TIP30 forms an intermolecular disulfide bridge (conformational change). TIP30 blocks the nuclear import of the mRNA-binding protein HuR by disrupting HuR–importin β2 association; elevated cytoplasmic HuR then binds the p53 mRNA 3'-UTR, prolonging p53 mRNA half-life and increasing p53 expression and transcriptional activity. TIP30-induced apoptosis and mitochondrial dysfunction are blocked by p53 silencing. |
Overexpression, siRNA knockdown of p53/HuR, mRNA stability assay, co-immunoprecipitation (HuR–importin β2), disulfide bridge analysis under oxidative stress, antioxidant/oxidant treatment, mitochondrial dysfunction assay |
Cancer research |
High |
18519672
|
| 2008 |
Abnormal overexpression of TIP30 in oligodendrocyte precursor cells (OPCs) in MS lesions traps NICD (Notch1 intracellular domain) and other NLS-bearing proteins with importin in the cytoplasm, blocking nuclear translocation required for myelinogenesis. Overexpression of TIP30 in a rat OPC cell line causes cytoplasmic entrapment of NICD and arrests differentiation upon Contactin-Fc stimulation. |
Immunohistochemistry in human MS tissue, overexpression in rat OPC cell line, functional differentiation assay |
The Journal of clinical investigation |
Medium |
19104151
|
| 2011 |
TIP30 forms a protein complex with endophilin B1 and ACSL4 that interacts with Rab5a. This TIP30 complex is required for proper endocytic trafficking of EGF-EGFR. Knockdown of TIP30, ACSL4, endophilin B1, or Rab5a traps EGF-EGFR in early endosomes, causing delayed EGFR degradation and prolonged EGFR signaling. The TIP30 complex facilitates trafficking of Rab5a and V-ATPases from the trans-Golgi network to EEA1-positive early endosomes in response to EGF. |
Co-immunoprecipitation, siRNA knockdown, genetic knockout (Tip30−/− primary hepatocytes), endosomal trafficking assay, colocalization with V-ATPases and EEA1 |
The Journal of biological chemistry |
High |
21252234
|
| 2011 |
The TIP30 protein complex (TIP30, ACSL4, endophilin B1) facilitates fusion of endocytic vesicles with Rab5a vesicles in vitro. Fusion depends on arachidonic acid, coenzyme A, and arachidonyl-CoA synthesis by ACSL4. The TIP30 complex transfers arachidonyl groups onto phosphatidic acid (PA), producing a lipid species that induces close membrane contact. |
In vitro vesicle fusion assay, arachidonyl-CoA synthesis assay, lipid transfer assay |
PloS one |
High |
21731680
|
| 2012 |
TIP30 loss in lung adenocarcinoma cells results in prolonged EGFR activity in early endosomes, delayed EGFR degradation, and increased EGFR nuclear localization, leading to upregulated pAKT and pERK1/2. Tip30 deletion in mice leads to spontaneous lung adenomas and adenocarcinomas, preceded by aberrant expansion of bronchioalveolar stem/progenitor and AT2 cells and increased EGFR expression. |
siRNA knockdown, Tip30 knockout mice, endosomal trafficking assay, Western blotting for EGFR signaling, nuclear EGFR localization, mouse tumor pathology |
Oncogene |
High |
22733137
|
| 2012 |
Sorafenib downregulates HTATIP2 expression in HCC cells via JAK-STAT3 signaling, promoting invasiveness and metastatic potential. HTATIP2 knockdown reduces sorafenib-promoted invasion, while HTATIP2 overexpression enhances it; HTATIP2 expression is associated with sorafenib-induced EMT. |
PCR arrays, shRNA knockdown, transgenic overexpression, orthotopic mouse model, Western blotting for JAK-STAT3 pathway, EMT marker analysis |
Gastroenterology |
Medium |
22922424
|
| 2012 |
TIP30 directly binds the DNA-binding domain and the C-terminal domain of p53 protein, as demonstrated by GST pull-down assay and surface plasmon resonance. |
GST pull-down assay, surface plasmon resonance (SPR) |
Molecules and cells |
Medium |
23178973
|
| 2013 |
miR-10b directly targets TIP30 mRNA (confirmed by luciferase reporter assay with 3'-UTR); miR-10b-mediated suppression of TIP30 enhances EGF-dependent EGFR tyrosine phosphorylation and ERK phosphorylation in pancreatic cancer cells. The effects of miR-10b are abrogated by expressing a modified TIP30 cDNA resistant to miR-10b. TIP30 silencing mimics miR-10b effects on invasion. |
Luciferase reporter assay, siRNA knockdown, miR-10b overexpression, EGFR/ERK phosphorylation (Western blotting), Matrigel invasion assay, rescue with miR-10b-resistant TIP30 |
Oncogene |
High |
24096486
|
| 2014 |
TIP30 inhibits EMT and nuclear accumulation of Snail in HCC cells by competitively interrupting the interaction of Snail with importin-β2, thereby blocking Snail nuclear import. Small interfering RNAs targeting Snail attenuate the EMT and tumor-initiating properties induced by TIP30 deficiency. |
Overexpression/knockdown, Co-immunoprecipitation (TIP30–importin-β2–Snail complex), nuclear fractionation, siRNA epistasis, in vitro and in vivo invasion/EMT assays |
Oncogene |
High |
24681951
|
| 2014 |
TIP30 translocates to the nucleus of lung adenocarcinoma cells in response to EGF treatment (via EGFR signaling); nuclear TIP30 negatively regulates EGF-dependent transcriptional activation of CCND1 (cyclin D1) through an HDAC1-dependent mechanism, as demonstrated by chromatin immunoprecipitation. |
Nuclear fractionation/localization, EGFR pathway inhibitor treatment, chromatin immunoprecipitation (ChIP), gene expression analysis |
Cancer letters |
Medium |
25135222
|
| 2014 |
TIP30 inhibits oligodendrocyte precursor cell (OPC) differentiation by sequestering the transcription factor Olig1 in the cytoplasm via direct interaction with Olig1, preventing its nuclear translocation. Overexpression of TIP30 sequesters Olig1 in the cytoplasm; knockdown of TIP30 increases nuclear Olig1 and enhances OPC differentiation. Tip30−/− mice display increased myelin protein levels at postnatal days 14 and 21. |
Primary OPC culture, overexpression and siRNA knockdown, Co-immunoprecipitation (TIP30–Olig1), nuclear/cytoplasmic fractionation, Tip30−/− mice, cuprizone demyelination model |
Glia |
High |
25530119
|
| 2015 |
TGF-β1 induces epigenetic silencing of TIP30 promoter via DNMT1 and DNMT3A upregulation (hypermethylation), reducing TIP30 expression during EMT. TIP30 silencing activates nuclear translocation and transcriptional activation of β-catenin in an AKT-dependent manner, promoting EMT in esophageal carcinoma cells. |
Promoter methylation analysis, DNMT knockdown/overexpression, Western blotting for AKT/β-catenin signaling, nuclear fractionation, in vitro and in vivo invasion assays |
Oncotarget |
Medium |
25544767
|
| 2017 |
TIP30 deficiency activates the Akt/mTOR signaling pathway, leading to upregulation and nuclear accumulation of SREBP1, which promotes transcription of lipogenesis genes (fasn, scd) and elevated fatty acid synthesis in HCC cells. siRNA targeting SREBP1 reverses the fatty acid synthesis induced by TIP30 deficiency. |
siRNA knockdown, Western blotting for Akt/mTOR/SREBP1 signaling, nuclear fractionation, fatty acid synthesis assay, siRNA epistasis |
Oncogenesis |
Medium |
28604762
|
| 2018 |
HIV-1 Tat protein interacts with TIP30 and blocks TIP30's binding to importin-β, thereby preventing TIP30-mediated inhibition of Snail nuclear import in lung cancer cells. Loss of TIP30-importin-β interaction (via Tat) increases nuclear Snail, promoting EMT and invasion. |
Co-immunoprecipitation (Tat–TIP30–importin-β), nuclear fractionation of Snail, overexpression, in vivo metastasis assay, immunohistochemistry |
Cancer science |
Medium |
30099830
|
| 2019 |
TIP30 binds eukaryotic elongation factor 1A (eEF1A) and prevents its interaction with co-factor eEF1B2, thereby inhibiting translational elongation and cardiac protein synthesis. Therapeutic overexpression of TIP30 in mouse hearts inhibits cardiac hypertrophy and improves left ventricular function during pressure overload and in mdx cardiomyopathic mice. Reduced TIP30 in Tip30-reduced mice leads to exaggerated cardiac growth and dysfunction during pressure overload; pharmacological inhibition of protein synthesis rescues these defects. |
Co-immunoprecipitation (TIP30–eEF1A), eEF1A–eEF1B2 interaction assay, in vivo cardiac-specific overexpression and KO mouse models, protein synthesis measurement, pressure-overload model, pharmacological inhibition rescue |
EMBO molecular medicine |
High |
31468715
|
| 2023 |
Epigenetic silencing of HTATIP2 in glioblastoma leads to enhanced nuclear localization of the base excision repair enzyme MPG (N-methylpurine DNA glycosylase). Induction of HTATIP2 expression shifts MPG from nuclear to cytoplasmic, while depletion of endogenous HTATIP2 increases nuclear MPG. Reduced nuclear MPG (via HTATIP2 induction or MPG depletion) yields fewer phospho-H2AX-positive cells upon alkylating agent treatment, indicating reduced BER capacity and fewer AP sites. |
HTATIP2 induction/knockdown, nuclear/cytoplasmic fractionation for MPG, phospho-H2AX assay after alkylating agent treatment, MPG knockdown epistasis |
Molecular oncology |
Medium |
37491696
|
| 2023 |
Increased HTATIP2 expression in proarteriogenic monocytes/macrophages from patients with chronic limb-threatening ischemia (CLTI) impairs their arteriogenic capacity. Silencing HTATIP2 in CLTI monocytes/macrophages restores expression of arteriogenic regulators Neuropilin-1 and Angiopoietin-1 and rescues their capacity to enhance angiogenic and arteriogenic processes in vitro and limb perfusion in vivo. |
siRNA knockdown in primary patient-derived monocytes/macrophages, endothelial tubule formation assay, smooth muscle proliferation assay, hindlimb ischemia in vivo model, Western blotting |
JCI insight |
Medium |
37847559
|
| 2010 |
Silencing of CC3/TIP30 expression strongly improves tumor cell survival under glucose limitation, enabling superior metabolic adaptation. CC3-silenced HeLa cells maintain higher mitochondrial respiration, higher expression of mitochondrial respiratory complex proteins, higher c-MYC and PKM2 (M2 isoform of pyruvate kinase) in low glucose, and fail to fully activate AMPK in response to glucose limitation. Pharmacological or siRNA inhibition of AMPK similarly protects control HeLa cells from glucose-limitation-induced death. |
siRNA knockdown of CC3, cell survival assay under glucose limitation, mitochondrial respiration measurement, Western blotting, AMPK pharmacological and siRNA inhibition |
Cell cycle (Georgetown, Tex.) |
Medium |
21150275
|
| 2010 |
Forced expression of CC3/TIP30 in CC3-negative cells strongly delays repair of UV-induced DNA damage, negatively affects expression of DDB2/XPE and p21CIP1, and inhibits nuclear accumulation of p21CIP1 after UV. Silencing endogenous CC3 significantly reduces translesion DNA synthesis after UV. CC3 expression also inhibits repair of oxidative DNA damage and decreases nucleoredoxin levels. |
Overexpression, siRNA knockdown, UV-induced DNA damage repair assay, Western blotting for DDB2/p21, nuclear fractionation, oxidative damage repair assay |
BMC cell biology |
Medium |
20374651
|
| 2024 |
TIP30 modulates mTORC1 signaling during CVB3 infection in HeLa cells. TIP30 overexpression mitigates CVB3-induced cellular pathogenesis; rapamycin (mTOR1 inhibitor) reverses these protective effects, indicating TIP30 acts upstream of mTORC1. TIP30-knockout mice show heightened heart virus titers and cardiac damage after CVB3 infection. |
TIP30 lentiviral overexpression, TIP30 knockout mice, rapamycin pharmacological epistasis, viral titer assay, Western blotting for mTORC1 pathway |
Virology |
Medium |
38981316
|
| 2025 |
Human TIP30 functionally complements yeast Fmp52 (a short-chain dehydrogenase/reductase at the ER) in protecting against lipid-induced apoptosis triggered by the sphingolipid-derived fatty aldehyde t-2-hex, indicating an evolutionarily conserved protective role for TIP30 at the ER against lipid-mediated cytotoxicity. |
Functional complementation in yeast (Fmp52 deletion rescued by human TIP30 expression), yeast apoptosis assay |
bioRxivpreprint |
Low |
bio_10.1101_2025.12.01.691522
|