PDCD4 inhibits translation initiation by binding to eIF4A using both its MA3 domains

S6K1- and ßTRCP-Mediated Degradation of PDCD4 Promotes Protein Translation and Cell Growth

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The Transformation Suppressor Pdcd4 Is a Novel Eukaryotic Translation Initiation Factor 4A Binding Protein That Inhibits Translation

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Human Eukaryotic Translation Initiation Factor 4G (eIF4G) Possesses Two Separate and Independent Binding Sites for eIF4A

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Bidirectional RNA Helicase Activity of Eucaryotic Translation Initiation Factors 4A and 4F

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Eukaryotic Translation Initiation Factor 4E (eIF4E) Binding Site and the Middle One-Third of eIF4GI Constitute the Core Domain for Cap-Dependent Translation, and the C-Terminal One-Third Functions as a Modulatory Region

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Atheroprotective Pulsatile Flow Induces Ubiquitin-Proteasome–Mediated Degradation of Programmed Cell Death 4 in Endothelial Cells

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Examining weak protein–protein interactions in start codon recognition via NMR spectroscopy

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Programmed cell death factor 4-mediated hippocampal synaptic plasticity is involved in early life stress and susceptibility to depression

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GADD45A suppression contributes to cardiac remodeling by promoting inflammation, fibrosis and hypertrophy

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The asymmetric syntheses of cryptocaryols A and B

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Programmed cell death 4 protein (Pdcd4) and homeodomain-interacting protein kinase 2 (Hipk2) antagonistically control translation of Hipk2 mRNA

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Translating from cancer to the brain: regulation of protein synthesis by eIF4FPreprint

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PDCD4 deficiency in hepatocytes exacerbates nonalcoholic steatohepatitis through enhanced MHC class II transactivator expression

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A Strategy for Full Interrogation of Prognostic Gene Expression Patterns: Exploring the Biology of Diffuse Large B Cell Lymphoma

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Programmed cell death 4 mechanism of action: The model to be updated?

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PDCD4 triggers α-synuclein accumulation and motor deficits via co-suppressing TFE3 and TFEB translation in a model of Parkinson’s disease

Cao, B., Chen, X., Li, Y., Zhou, T., Chen, N., Guo, Y., Zhao, M., Guo, C., Shi, Y., Wang, Q., et al. (2024) · npj Parkinson's Disease · doi:10.1038/s41531-024-00760-9 · Cited by 8

Molecular cloning, inducible expression with SGIV and Vibrio alginolyticus challenge, and function analysis of Epinephelus coioides PDCD4

Chen, G., Li, P.-H., He, J., Su, Y., Chen, H.-J., Dong, J., Huang, Y., Huang, X., Jiang, Y., Qin, Q., et al. (2021) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2021.104013 · Cited by 8

Exopolysaccharide of Levilactobacillus brevis M-10 Improved Physiological and Biochemical Indicators and Gut Microbiota in DSS-Induced Colitis Mice

Wang, Q., Zhang, W., Liu, J., Qin, W., & Cai, J. (2025) · Current Microbiology · doi:10.1007/s00284-025-04190-5 · Cited by 8

Programmed cell death 4 inhibits proliferation and differentiation and induces apoptosis of human mesenchymal stem cells through suppressing the Wnt/β-catenin pathway

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Tumor Suppressor p53 Down-Regulates Programmed Cell Death Protein 4 (PDCD4) Expression

Yang, W. H., George, A. P., Wang, C., Yang, R. H., Duncan, A. M., Patel, D., Neil, Z. D., & Yang, W. (2023) · Current Oncology · doi:10.3390/curroncol30020124 · Cited by 6

Regulated by S6 Kinase 2 Translation of Antiapoptotic Proteins and Is Internal Ribosome Entry Site-Mediated Tumor Suppressor PDCD4 Represses

Holčík, M., Lewis, S. M., Pardo, O. E., Seckl, M. J., Liwak, U., Thakor, N., Jordan, L. E., & Roy, R. (2012) · Cited by 7

Distinct roles of different fragments of PDCD4 in regulating the metastatic behavior of B16 melanoma cells

Wang, D., Guo, S., Han, S., Xu, N., Guo, J., & Sun, Q. (2013) · International Journal of Oncology · doi:10.3892/ijo.2013.1841 · Cited by 6

In situ imaging and interfering Dicer-mediated cleavage process via a versatile molecular beacon probe

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90th Anniversary Commentary: The mTORC1 Complex—A Central Player in the Control and Regulation of Amino Acid Sufficiency

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Discovery of a sushi domain-containing protein 2-positive phenotype in circulating tumor cells of metastatic breast cancer patients

Bartkowiak, K., Mohammadi, P. M., Nissen, P., Werner, S., Agorku, D., Andreas, A., Geffken, M., Peine, S., Verpoort, K., Deutsch, T. M., et al. (2025) · Scientific Reports · doi:10.1038/s41598-025-87122-4 · Cited by 5

Regulation of Apoptotic Pathways by MicroRNAs: A Therapeutic Strategy for Alzheimer’s Disease

Saadh, M. J., Muhammad, F. A., Alazzawi, T. S., Fahdil, A. A., Athab, Z. H., Tuxtayev, J., Alsaikhan, F., & Farhood, B. (2025) · Molecular Neurobiology · doi:10.1007/s12035-025-04833-5 · Cited by 5

Deciphering the role of siRNA in anxiety and depression

Bale, R., & Doshi, G. (2024) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2024.176868 · Cited by 3

Long noncoding RNA EPCART regulates translation through PI3K/AKT/mTOR pathway and PDCD4 in prostate cancer

Kohvakka, A., Sattari, M., Nättinen, J. E., Aapola, U., Gregorová, P., Tammela, T. L. J., Uusitalo, H. M. T., Sarin, L. P., Visakorpi, T., & Latonen, L. (2024) · Cancer Gene Therapy · doi:10.1038/s41417-024-00822-3 · Cited by 4

Leucine-Induced Upregulation of Terminal Oligopyrimidine mRNA Translation in Skeletal Muscle: Just the Tip of the Iceberg?

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Resonance assignment and secondary structure of the middle MA-3 domain and complete tandem MA-3 region of the tumour suppressor protein Pdcd4

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The Dynamic Life with DEAD-Box RNA Helicases

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PDCD4

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Diverse Mechanisms of Translation Regulation and Their Role in Cancer

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RSK1 and RSK2 modulate the translatome of glioblastoma cells in an isoform-specific and mTORC1 independent manner

Roffé, M., Nascimento, D. P., Nunes, P. B. C., Soares, L. C., Alves, A. H., Hamraghani, A., Almasi, Y., Djaoud, Z., Hajj, G. N. M., Martins, V. R., et al. (2025) · Neuro-Oncology Advances · doi:10.1093/noajnl/vdaf144 · Cited by 2

A novel programmed cell death protein 4 negatively regulates CgIL17-5 expression in hemocytes of oyster Pacific oyster (Crassostrea gigas)

Yan, Y., Wang, W., Liu, Z., Lv, X., Li, M., Yang, W., Wang, L., & Song, L. (2020) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2020.02.038 · Cited by 2

PIM kinase control of CD8 T cell protein synthesis and cell trafficking

Marchingo, J. M., Spinelli, L., Pathak, S., & Cantrell, D. A. (2025) · eLife · doi:10.7554/elife.98622.3 · Cited by 2

Aberrant translation of proteins implicated in Alzheimer�s disease pathology

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CRISPRδ: dCas13-mediated translational repression for accurate gene silencing in mammalian cellsPreprint

Apostolopoulos, A., Tsuiji, H., Shichino, Y., & Iwasaki, S. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.14.540671 · Cited by 2

Mutant NPM1 modulates PDCD4 ubiquitination degradation and facilitates leukemogenesis

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Functional characterisation of tumour suppressor PDCD4 reveals previously undisclosed role in the control of cell adhesion

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mTORC1: A Signaling Integration Node Involved in Cell Growth

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Regulation and dysregulation of protein synthesis in cancer cells

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PIM kinase control of CD8 T cell protein synthesis and cell traffickingPreprint

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A proteomic map of B cell activation and its shaping by mTORC1, MYC and ironPreprint

James, O., Sinclair, L. V., Lefter, N., Brock, A. A. C., Salerno, F., Brenes, A. J., Khameneh, H. J., Pecoraro, M., Guarda, G., & Howden, A. J. M. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.12.19.629506 · Cited by 2

Downstream from mTOR: Therapeutic Approaches to Targeting the eIF4F Translation Initiation Complex

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Analyse fonctionnelle de la traduction dépendante de la coiffe m⁷GTP en réponse à la fécondation et au cours du cycle cellulaire de l'embryon d'oursin

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Alterations in the regulatory networks of cellular and molecular events

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Peroxynitrite-induced apoptosis in human brain vascular smooth muscle cells is associated with induction of PDCD4 gene expression

Li, Y., Li, L., Jiao, Y., Xu, C., Zhang, G., Liu, W., Yue, Z., & Li, J. (2012) · Biomedical Research-tokyo

Estudio de la regulación del factor de iniciación de la traducción eIF4E mediante su interacción con la proteína CERES

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Exogenous Alpha-Synuclein Induces Cell Death Related Proteins in C6 Oligodendrocyte-Like Cells Corresponding to Protein Expression Observed in Multiple System Atrophy

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Data from Targeting Oncogene mRNA Translation in B-Cell Malignancies with eFT226, a Potent and Selective Inhibitor of eIF4A

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Eukaryotic Initiation Factor 3F (eIF3F) Regulates the IRES-Mediated Translation of Bcl-xL via Its Interaction with Programmed Cell Death 4 (PDCD4) Protein

Hegde, V., Sharma, D. K., Patel, H., Narasimha, P. L., Luddu, J., Mubaya, R., Holčík, M., & Thakor, N. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27093955

Opticool: Cutting-edge transgenic optical tools

Fenelon, K. D., Krause, J., & Koromila, T. (2024) · PLoS Genetics · doi:10.1371/journal.pgen.1011208

Human tumor suppressor protein Pdcd4 binds at the mRNA entry channel in 40S small ribosomal subunitPreprint

Querido, J. B., Sokabe, M., Díaz‐López, I., Gordiyenko, Y., Zuber, P. K., Du, Y., Albacete-Albacete, L., Ramakrishnan, V., & Fraser, C. S. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.05.01.592117

PIM kinase control of CD8 T cell protein synthesis and cell traffickingPreprint

Marchingo, J. M., Spinelli, L., Pathak, S., & Cantrell, D. A. (2024) · eLife · doi:10.7554/elife.98622.1

Translation Initiation Factor-2S2 (eIF2S2) Contributes to Cervical Carcinogenesis by Inhibiting the TGF-β/SMAD4 Signaling Pathway

Kundu, J., Yang, H., Moon, S., Byun, M. R., Shin, Y. K., Song, K., & Choi, J. (2024) · Biomolecules & Therapeutics · doi:10.4062/biomolther.2024.024

Targeting the translation initiation complex in therapy-resistant and metastatic melanomaPreprint

Feng, Y., Diaz-Olea, X., Ke, X., Radaeva, M., Amiri, M., Joo, H., Jafari, M., Kim, H., Deshpande, A. J., Olson, S. H., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.11.20.624566

PIM kinase control of CD8 T cell protein synthesis and cell traffickingPreprint

Marchingo, J. M., Spinelli, L., Pathak, S., & Cantrell, D. A. (2025) · eLife · doi:10.7554/elife.98622.2

Covalent Inhibition of the Peptidyl‐Prolyl Isomerase Pin1 by Sulfopin Results in a Broad Impact on the Phosphoproteome of Human Osteosarcoma U2‐OS Cells

Roffey, S. E., Hovey, O. F. J., Jurčić, K., Lu, K. P., Zhou, X. Z., & Litchfield, D. W. (2025) · PROTEOMICS · doi:10.1002/pmic.13980

IGF1R-targeted delivery of a bridged nucleic acid oligonucleotide-peptide conjugate for microRNA-21 inhibition in triple-negative breast cancer

Jin, Y., Desai, V., Mazzaroth, J., & Wickstrom, E. (2025) · NAR Cancer · doi:10.1093/narcan/zcaf053

Implication du complexe d'initiation de la traduction eIF4F dans la résistance aux inhibiteurs de la voie des MAPK

Malka-Mahieu, H. (2015) · theses.fr (ABES) · doi:10.70675/0885c423zadabz4b67zad92zc16c642a3d08

Etude de l’implication du complexe eIF4F dans la réponse immune antitumorale via la régulation traductionnelle de l’axe STAT1-PD-L1 dans le mélanome métastatique

Guemiri, R. (2018) · theses.fr (ABES) · doi:10.70675/907b71d5z497ez45c1za40azfb52b263aeb7

Recherche de biomarqueurs pronostiques dans le mélanome muqueux non opérable et/ou métastatique : Régulation traductionnelle de SOX10 par l’hexokinase 2 et modulation de l'agressivité tumorale dans le mélanome cutané

Moya‐Plana, A. (2020) · theses.fr (ABES) · doi:10.70675/951feb6cz54bez4481zb3a9z590aa53175b4

Translatome-based classification of pancreatic cancer

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Structural and functional characterisation of the 5’ untranslated regions of β-catenin and HIF-1α mRNAs and their translational role in cancer cells under hypoxia

Moreno, J. R. (2022) · theses.fr (ABES) · doi:10.70675/21df9a0cz08ccz48fez9d50ze08a54d8e3c7

PDCD4 as tumor suppressor protein in gastric mucosa in early, advanced precancerous lesions and gastric adenocarcinoma

Кононов, А. В., Рубцов, В. А., Поморгайло, Е. Г., Mozgovoi, S. I., Геннадьевна, Ш. А., & Маркелова, М. В. (2026) · Russian Journal of Archive of Pathology · doi:10.17116/patol2026880216

PDCD4-driven steatosis via the HNF4A/GK axis is attenuated by the natural compound isosinensetin

Cheng, X., Lu, K., Yang, L., Cheng, K., Chen, Q., Zhao, R., Niu, J., Cheng, R., Wang, J., Wu, L., et al. (2026) · Phytomedicine · doi:10.1016/j.phymed.2026.158810

Programmed cell death protein 4 (PDCD4): a pleiotropic regulator in cardiovascular diseases

Zheng, M., & Jiang, X. (2026) · Journal of Physiology and Biochemistry · doi:10.1007/s13105-026-01237-4

Histology-Stratified Clinical and Prognostic Associations of PDCD-Related Genes in Lung Adenocarcinoma and Lung Squamous Cell Carcinoma

Kim, S.-T., Lee, Y., Yun, S.-Y., Min, J.-W., Jeon, E.-C., Kim, S., Yoo, J.-S., Park, S.-J., Jung, J.-H., Lee, J.-C., et al. (2026) · Genes · doi:10.3390/genes17101238

Using Solution NMR to Study the RNA-Binding Properties and Molecular Mechanisms of the RNA Helicase DDX3X

Toyama, Y., Takeuchi, K., & Shimada, I. (2026) · Methods in molecular biology · doi:10.1007/978-1-0716-5571-9_18

Structural Basis for Inhibition of Translation by the Tumor Suppressor Pdcd4

LaRonde-LeBlanc, N. A., Santhanam, A. N., Baker, A. R., Wlodawer, A., & Colburn, N. H. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.00867-06 · Cited by 76

A Novel Function of the MA-3 Domains in Transformation and Translation Suppressor Pdcd4 Is Essential for Its Binding to Eukaryotic Translation Initiation Factor 4A

Yang, H.-S., Cho, M.-H., Zakowicz, H., Hegamyer, G., Sonenberg, N., & Colburn, N. H. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.9.3894-3906.2004 · Cited by 199

Structure of the C-terminal MA-3 domain of the tumour suppressor protein Pdcd4 and characterization of its interaction with eIF4A

Waters, L. C., Veverka, V., Böhm, M., Schmedt, T., Choong, P. T., Muskett, F. W., Klempnauer, K.-H., & Carr, M. D. (2007) · Oncogene · doi:10.1038/sj.onc.1210305 · Cited by 49

Crystal structure of the eIF4A–PDCD4 complex

Chang, J. H., Cho, Y. H., Sohn, S. Y., Choi, J. M., Kim, A., Kim, Y. C., Jang, S. K., & Cho, Y. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0808275106 · Cited by 120

Structural basis for translational inhibition by the tumour suppressor Pdcd4

Loh, P. G., Yang, H., Walsh, M. A., Wang, Q., Wang, X., Cheng, Z., Liu, D. X., & Song, H. (2009) · The EMBO Journal · doi:10.1038/emboj.2008.278 · Cited by 128