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GENE:

MIR196B (MicroRNA 196b)

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Other names: MIR196B, MicroRNA 196b, Hsa-MiR-196b-3p, Hsa-MiR-196b-5p, Hsa-Mir-196b, MIRN196B, Hsa-Mir-196-P3, MIMAT0001080, MIMAT0009201, MiRNA196B, MI0001150, MiR-196b, RF00256
Associations
Trials
27d
MicroRNAs in Esophageal Cancer: Implications for Diagnosis, Progression, Prognosis and Chemoresistance. (PubMed, Int J Mol Sci)
Moreover, distinct miRNA expression patterns are correlated with tumor aggressiveness, metastatic potential, and the risk of recurrence, supporting their integration with conventional histopathological and molecular parameters for improved patient stratification. Overall, miRNAs represent a powerful class of biomarkers and potential therapeutic targets in EC, with increasing translational relevance in precision oncology.
Review • Journal
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MIR21 (MicroRNA 21) • MIR23A (MicroRNA 23a) • MIR196B (MicroRNA 196b) • MIR455 (MicroRNA 455)
1m
Diagnostic efficacy of blood biomarkers for differentiating early-stage pancreatic cancer from chronic pancreatitis: A systematic review and network meta-analysis. (PubMed, Transl Oncol)
CA199 demonstrated only moderate diagnostic discrimination between PC and CP, with reduced efficacy in early-stage PC. Combining CA199 and eight exLRs exhibited promising differential diagnostic efficacy with both high sensitivity and specificity.
Retrospective data • Review • Journal
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CEACAM5 (CEA Cell Adhesion Molecule 5) • CA 19-9 (Cancer antigen 19-9) • MIR196B (MicroRNA 196b)
2ms
miR-196b-5p Targets TGFBR3 to Reinforce the Invasion and Migration of LUAD Cells. (PubMed, J Biochem Mol Toxicol)
miR-196b-5p in LUAD cells targeted to downregulate TGFBR3 to enhance cell invasion and migration. In summary, our study reveals that miR-196b-5p targets and downregulates TGFBR3, thereby boosting the migration and invasion of LUAD cells.
Journal
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TGFB1 (Transforming Growth Factor Beta 1) • MIR196B (MicroRNA 196b)
4ms
MicroRNA profiling of testicular Leydig cell tumors identifies a microRNA signature associated with malignancy and miR-196b-5p as a potentially useful biomarker. (PubMed, J Pathol)
© 2025 The Author(s). The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland
Journal
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MIR196B (MicroRNA 196b)
5ms
Differential expression of miRNAs in primary canine appendicular osteosarcoma tissue and pulmonary metastases. (PubMed, Vet Pathol)
This study found miRNAs that are nearly exclusively expressed in metastatic pulmonary OSA and could serve as novel therapeutic targets. MiRNAs were also found to be important prognostic biomarkers in tissue and improved prognostic ability as miRNA signatures.
Journal
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MIR196B (MicroRNA 196b)
5ms
MicroRNA 196a contributes to the aggressiveness of esophageal adenocarcinoma through the MYC/TERT/NFκB axis. (PubMed, Mol Oncol)
These effects are dependent on the c-MYC/TERT/NFκB signaling molecular axis. BE patients and non-invasive EAC patients with high miR-196a expression could benefit from therapeutic interventions to prevent EMT or activation of the molecular pathway described in this study.
Journal
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MYC (V-myc avian myelocytomatosis viral oncogene homolog) • TERT (Telomerase Reverse Transcriptase) • MIR192 (MicroRNA 192) • NFKBIA (NFKB Inhibitor Alpha 2) • MIR196A1 (MicroRNA 196a-1) • MIR196B (MicroRNA 196b) • VCP (Valosin Containing Protein)
7ms
Evaluation of HOTAIRM1, miR-196b, and HOXA9 as Oncogenic Markers in Patients with Acute Myeloblastic Leukemia. (PubMed, Iran J Pathol)
Furthermore, t-test analysis revealed that the expressions of HOTAIRM1, HOXA9, and GFI1 significantly differed between AML-M3 and non-M3 AML subtypes. These findings suggest that the investigated markers, particularly HOTAIRM1, HOXA9, and GFI1, may serve as potential clinical biomarkers for monitoring AML progression and could be valuable targets for early detection or therapeutic intervention.
Journal
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HOXA9 (Homeobox A9) • PIM1 (Pim-1 Proto-Oncogene) • MIR196B (MicroRNA 196b)
8ms
CAF-derived exosomal miR-196b-5p after androgen deprivation therapy promotes epithelial-mesenchymal transition in prostate cancer cells through HOXC8/NF-κB signaling pathway. (PubMed, Biol Direct)
Our study elucidates a specific mechanism by which CAF-derived exosomes promote prostate cancer metastasis via miR-196b-5p regulation, contributing to the identification of therapeutic targets for managing tumor metastasis following castration.
Journal
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HOXC8 (Homeobox C8) • MIR196B (MicroRNA 196b)
8ms
Omics Study of Ovarian Malignancies: From Urine Metabolomic Profile to Minimally Invasive MicroRNA Markers (PubMed, Mol Biol (Mosk))
Thus, significant metabolomic imbalance in the urine was observed in the OC patients and was associated with changes in the levels of microRNAs that regulate the signaling pathways of the metabolites. The 26 compounds with abnormal concentrations and the levels of the microRNAs miR-33b-5p, miR-423-5p, miR-6843-3p, miR-4668-3p, miR-30c-5p, miR-6743-5p, miR-4742-5p, miR-1207-5p, and miR-17-5p in the urine were considered to be suitable as noninvasive diagnostic markers of OC.
Journal • Metabolomic study
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MIR27A (MicroRNA 27a) • MIR17 (MicroRNA 17) • MIR23A (MicroRNA 23a) • MIR370 (MicroRNA 370) • MIR1207 (MicroRNA 1207) • MIR181A1 (MicroRNA 181a-1) • MIR181B1 (MicroRNA 181b-1) • MIR196B (MicroRNA 196b) • MIR19A (MicroRNA 19a) • MIR208A (MicroRNA 208a) • MIR29A (MicroRNA 29a) • MIR30C • MIR330 (MicroRNA 330) • MIR423 (MicroRNA 423) • MIR4742 (MicroRNA 4742) • MIR653 (MicroRNA 653) • MIRLET7B (MicroRNA Let-7b)
8ms
microRNA-196b-5p expression in cancer tissues is closely associated with clinical and pathological characteristics and prognosis of patients with non-small cell lung cancer. (PubMed, J Cardiothorac Surg)
High miR-196b-5p expression in cancer tissues of NSCLC patients was closely linked to capsule invasion, LNM, maximum tumor diameter, and clinical TNM stage and was an IRF for 3-year postoperative mortality in NSCLC patients.
Retrospective data • Journal
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MIR196B (MicroRNA 196b)
9ms
miR-196b strictly regulates and reliably predicts the response to cetuximab in colorectal cancer. (PubMed, Cell Mol Biol Lett)
This study supports that activation of the ERK signaling pathway is a key factor in cetuximab resistance. In addition, miR-196b can modulate and predict the CRC response to cetuximab, holding broad potential applications.
Journal
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BRAF (B-raf proto-oncogene) • NRAS (Neuroblastoma RAS viral oncogene homolog) • MIR196B (MicroRNA 196b)
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Erbitux (cetuximab)
10ms
Catalytic hairpin assembly-powered nanozyme-SERS dual-function sensing system for ultrasensitive detection of gastric precancerous lesions. (PubMed, Biosens Bioelectron)
Introducing Receiver Operating Characteristic (ROC) curves to evaluate the diagnostic efficacy of sensing system in detecting precancerous lesions of gastric cancer, the area under the curve (AUC) values for target combination diagnosis were 0.954 and 0.957, respectively. Therefore, the proposed dual function sensing system has broad application prospects in the clinical detection of precancerous lesions of gastric cancer.
Journal
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MIR221 (MicroRNA 221) • MIR196B (MicroRNA 196b)