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MDM2 and breast cancer are reported together in 9 articles.
Gene
MDM2
- HGNC
- HGNC:6973
48articles
48mentions
5variants with confirmed gene link
Most co-reported phenotypes (articles)
breast cancer 9colorectal cancer 3prostate cancer 3hepatocellular carcinoma 2Alzheimer disease 1leukemia 1lung cancer 1ovarian cancer 1
Reported variants (articles · ClinVar status)
Phenotype
Breast cancer
1,211articles
1,211mentions
12co-reported genes shown
Most co-reported genes (articles)
Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.
Publications
9 records shown · first 60Cohesive data analysis for the identification of prognostic hub genes and significant pathways associated with HER2 + and TN breast cancer types.
PMID 40604083 | PMCID PMC12222827 | DOI 10.1038/s41598-025-94084-0 · Scientific reports · 2025 · 12 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | MDM2 | “Ten hub genes were obtained based on maximum clique centrality (MCC), maximum neighborhood component (MNC), degree, closeness and betweenness using cytoHubba which included ACTB, ATM, ESR1, GAPDH, HNRNPK, KRAS, MDM2, SIRT1, TP53, and H3F3C (H3-5).” | 0.98 | hgnc_dict_v1 |
| phenotype | breast cancer | “Cohesive data analysis for the identification of prognostic hub genes and significant pathways associated with HER2 + and TN breast cancer types.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | MCC | “Ten hub genes were obtained based on maximum clique centrality (MCC), maximum neighborhood component (MNC), degree, closeness and betweenness using cytoHubba which included ACTB, ATM, ESR1, GAPDH, HNRNPK, KRAS, MDM2, SIRT1, TP53, and H3F3C (H3-5).” | 0.98 | hgnc_dict_v1 |
| gene | ACTB | “Ten hub genes were obtained based on maximum clique centrality (MCC), maximum neighborhood component (MNC), degree, closeness and betweenness using cytoHubba which included ACTB, ATM, ESR1, GAPDH, HNRNPK, KRAS, MDM2, SIRT1, TP53, and H3F3C (H3-5).” | 0.98 | hgnc_dict_v1 |
Targeting MDM2-p53 interaction for breast cancer therapy.
PMID 40191734 | PMCID PMC11964874 | DOI 10.32604/or.2025.058956 · Oncology research · 2025 · 3 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | MDM2 | “To address this issue, advances have been made in therapies targeting molecular pathways related to the murine double minute 2 proto-oncogene (MDM2)-tumor proteinp53 (TP53) interaction.” | 0.98 | hgnc_dict_v1 |
| phenotype | breast cancer | “Targeting MDM2-p53 interaction for breast cancer therapy.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | TP53 | “To address this issue, advances have been made in therapies targeting molecular pathways related to the murine double minute 2 proto-oncogene (MDM2)-tumor proteinp53 (TP53) interaction.” | 0.98 | hgnc_dict_v1 |
Reinvestigation of Passerini and Ugi scaffolds as multistep apoptotic inducers via dual modulation of caspase 3/7 and P53-MDM2 signaling for halting breast cancer.
PMID 37736568 | PMCID PMC10509784 | DOI 10.1039/d3ra04029a · RSC advances · 2023 · 3 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | MDM2 | “The adopted design rationale and synthetic routes relied on mimicking the general thematic features of lead MDM2 inhibitors incorporating multiple aromatic rings.” | 0.98 | hgnc_dict_v1 |
| phenotype | breast cancer | “Reinvestigation of Passerini and Ugi scaffolds as multistep apoptotic inducers via dual modulation of caspase 3/7 and P53-MDM2 signaling for halting breast cancer.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | BAX | “Further apoptosis studies revealed that these compounds enhanced gene expression of BAX by 2 folds and suppressed Bcl-2 expression by 4.29-7.75 folds in the treated MCF-7 cells.” | 0.98 | hgnc_dict_v1 |
Novel spirooxindole based benzimidazole scaffold: In vitro, nanoformulation and in vivo studies on anticancer and antimetastatic activity of breast adenocarcinoma.
PMID 36174446 | DOI 10.1016/j.bioorg.2022.106124 · Bioorganic chemistry · 2022 · 2 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | MDM2 | “Also, it enhanced the protein expression of apoptotic marker p53 and moderate binding affinity for MDM2 (KD;7.94 μM).” | 0.98 | hgnc_dict_v1 |
| phenotype | breast cancer | “SP1 did halt the proliferation of breast cancer cells as well as suppressed the metastasis in other organs like liver, lung and heart.” | 0.98 | phenotype_alias_lexicon_v2 |
Murine Double Minute 2 Gene (MDM2) rs937283A/G variant significantly increases the susceptibility to breast cancer in Saudi Women.
PMID 33911942 | PMCID PMC8071807 | DOI 10.1016/j.sjbs.2021.01.020 · Saudi journal of biological sciences · 2021 · 5 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | MDM2 | “Murine Double Minute 2 Gene (MDM2) rs937283A/G variant significantly increases the susceptibility to breast cancer in Saudi Women.” | 0.98 | hgnc_dict_v1 |
| phenotype | breast cancer | “Murine Double Minute 2 Gene (MDM2) rs937283A/G variant significantly increases the susceptibility to breast cancer in Saudi Women.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | TP53 | “TP53 and its inhibitor the murine double minute 2 (MDM2) genes encode proteins that have crucial functions in the DNA damage response.” | 0.98 | hgnc_dict_v1 |
| population | Saudi Arabia | “Murine Double Minute 2 Gene (MDM2) rs937283A/G variant significantly increases the susceptibility to breast cancer in Saudi Women. In the present case-control study, the association of MDM2 rs937283A/G polymorphism and breast cancer susceptibility in Saudi women with samples of 137 breast cancer patients, and 98 healthy controls were explored. The results revealed that rs937283A/G variant is significantly increases the risk of breast cancer in Saudi women (p-value = 0.0078). Positive association between increased breast cancer risk and rs937283 variant in premenopausal Saudi women, below 50 years of age, was demonstrated (p-value = 0.0023). Collectively, MDM2 rs937283A/G polymorphism could act as a possible biomarker for breast cancer susceptibility in Saudi women.” | 0.95 | saudi_context_rules_v1 |
Clinical significance of TP53 (R72P) and MDM2 (T309G) polymorphisms in breast cancer patients.
PMID 26553387 | DOI 10.1007/s12094-015-1425-5 · Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2016 · 5 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | MDM2 | “Clinical significance of TP53 (R72P) and MDM2 (T309G) polymorphisms in breast cancer patients.” | 0.98 | hgnc_dict_v1 |
| phenotype | breast cancer | “Clinical significance of TP53 (R72P) and MDM2 (T309G) polymorphisms in breast cancer patients.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | TP53 | “Clinical significance of TP53 (R72P) and MDM2 (T309G) polymorphisms in breast cancer patients.” | 0.98 | hgnc_dict_v1 |
| variant | R72P | “Clinical significance of TP53 (R72P) and MDM2 (T309G) polymorphisms in breast cancer patients.” | 0.82 | literature_variant_regex_v2 |
Violacein induces apoptosis in human breast cancer cells through up regulation of BAX, p53 and down regulation of MDM2.
PMID 26521020 | DOI 10.1016/j.etp.2015.10.002 · Experimental and toxicologic pathology : official journal of the Gesellschaft fur Toxikologische Pathologie · 2016 · 4 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | MDM2 | “Violacein induces apoptosis in human breast cancer cells through up regulation of BAX, p53 and down regulation of MDM2.” | 0.98 | hgnc_dict_v1 |
| phenotype | breast cancer | “Violacein induces apoptosis in human breast cancer cells through up regulation of BAX, p53 and down regulation of MDM2.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | FADD | “Further, 0.45 and 4.5 μM of violacein increased apoptotic genes, such as Bax, p53, caspase 3, Fas, FADD and markedly reduced Bcl-2 and MDM2 expression levels to two fold when compared to control.” | 0.98 | hgnc_dict_v1 |
| gene | CDKN1A | “In addition violacein upregulated poly ADP-ribose polymerase (PARP), CDKN1A and caspase-9 significantly (p≤0.05) when compared to control.” | 0.98 | hgnc_dict_v1 |
A single-nucleotide polymorphism in the TP53 and MDM-2 gene modifies breast cancer risk in an ethnic Arab population.
PMID 21477265 | DOI 10.1111/j.1472-8206.2011.00939.x · Fundamental & clinical pharmacology · 2012 · 5 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | MDM2 | “The tumor suppressor TP53 and its negative regulator MDM2 play crucial roles in carcinogenesis.” | 0.98 | hgnc_dict_v1 |
| phenotype | breast cancer | “A single-nucleotide polymorphism in the TP53 and MDM-2 gene modifies breast cancer risk in an ethnic Arab population.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | TP53 | “A single-nucleotide polymorphism in the TP53 and MDM-2 gene modifies breast cancer risk in an ethnic Arab population.” | 0.98 | hgnc_dict_v1 |
| gene | TG | “We found an increased breast cancer risk associated with the MDM2 GG [odds ratio (OR) = 2.79, 95% confidence interval (CI) = 2.04-3.92] and TG [OR = 1.43, 95% CI = 1.12-2.02] genotypes.” | 0.98 | hgnc_dict_v1 |
Prognostic relevance of gene amplifications and coamplifications in breast cancer.
PMID 15574759 | DOI 10.1158/0008-5472.CAN-04-1945 · Cancer research · 2004 · 4 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | MDM2 | “Multiple different oncogenes have been described previously to be amplified in breast cancer including HER2, EGFR, MYC, CCND1, and MDM2.” | 0.98 | hgnc_dict_v1 |
| phenotype | breast cancer | “Prognostic relevance of gene amplifications and coamplifications in breast cancer.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | EGFR | “Multiple different oncogenes have been described previously to be amplified in breast cancer including HER2, EGFR, MYC, CCND1, and MDM2.” | 0.98 | hgnc_dict_v1 |
| gene | CCND1 | “Multiple different oncogenes have been described previously to be amplified in breast cancer including HER2, EGFR, MYC, CCND1, and MDM2.” | 0.98 | hgnc_dict_v1 |