Related Experiment Video
Updated: Nov 15, 2025

Analysis of Combinatorial miRNA Treatments to Regulate Cell Cycle and Angiogenesis
Published on: March 30, 2019
Regulation of ZMYND8 to Treat Cancer
Yun Chen1,2, Ya-Hui Tsai1,2, Sheng-Hong Tseng1,3
1Department of Surgery, Far Eastern Memorial Hospital, Pan-Chiao, New Taipei 220, Taiwan.
Abstract:
Zinc finger myeloid, nervy, and deformed epidermal autoregulatory factor 1-type containing 8 (Zinc finger MYND-type containing 8, ZMYND8) is a transcription factor, a histone H3-interacting protein, and a putative chromatin reader/effector that plays an essential role in regulating transcription during normal cellular growth. Mutations and altered expression of ZMYND8 are associated with the development and progression of cancer. Increased expression of ZMYND8 is linked to breast, prostate, colorectal, and cervical cancers. It exerts pro-oncogenic effects in breast and prostate cancers, and it promotes angiogenesis in zebrafish, as well as in breast and prostate cancers. In contrast, downregulation of ZMYND8 is also reported in breast, prostate, and nasopharyngeal cancers. ZMYND8 acts as a tumor suppressor in breast and prostate cancers, and it inhibits tumor growth by promoting differentiation; inhibiting proliferation, cell-cycle progression, invasiveness, and metastasis; and maintaining the epithelial phenotype in various types of cancers. These data together suggest that ZMYND8 is important in tumorigenesis; however, the existing data are contradictory. More studies are necessary to clarify the exact role of ZMYND8 in tumorigenesis. In the future, regulation of expression/activity of ZMYND8 and/or its binding partners may become useful in treating cancer.
Insights
Zinc finger MYND-type containing 8 (ZMYND8) has a dual role in cancer, acting as both an oncogene and tumor suppressor. Further research is needed to clarify its complex role in tumorigenesis and potential therapeutic applications.
Area of Science:
- Molecular Biology
- Cancer Research
- Epigenetics
Background:
- ZMYND8 is a transcription factor and chromatin regulator crucial for normal cellular processes.
- Altered ZMYND8 expression is implicated in various cancers, including breast, prostate, and colorectal.
- Its precise role in tumorigenesis remains unclear due to contradictory findings.
Purpose of the Study:
- To review the current understanding of ZMYND8's function in cancer.
- To highlight the contradictory roles of ZMYND8 as both an oncogene and tumor suppressor.
- To emphasize the need for further research into ZMYND8's mechanisms in tumorigenesis.
Main Methods:
- Literature review of studies investigating ZMYND8 in cancer.
- Analysis of ZMYND8's known functions as a transcription factor and chromatin regulator.
- Comparison of studies reporting increased versus decreased ZMYND8 expression in different cancer types.
Main Results:
- Increased ZMYND8 expression is linked to pro-oncogenic effects and angiogenesis in breast and prostate cancers.
- Downregulation of ZMYND8 is observed in breast, prostate, and nasopharyngeal cancers, where it acts as a tumor suppressor.
- ZMYND8's tumor-suppressive functions include promoting differentiation and inhibiting proliferation and metastasis.
Conclusions:
- ZMYND8 plays a significant, albeit complex and contradictory, role in tumorigenesis.
- Its dual function as an oncogene and tumor suppressor necessitates further investigation.
- Targeting ZMYND8 or its binding partners may offer future therapeutic strategies for cancer treatment.
More Related Videos
07:24Repression of Multiple Myeloma Cell Growth In Vivo by Single-wall Carbon Nanotube SWCNT-delivered MALAT1 Antisense Oligos
Published on: December 13, 2018
09:45Mosaic Zebrafish Transgenesis for Functional Genomic Analysis of Candidate Cooperative Genes in Tumor Pathogenesis
Published on: March 31, 2015
Related Concept Videos
Abnormal Proliferation
Receptor Downregulation in MVBs
The EGFR can initiate signaling pathways that lead to cell proliferation, migration, and differentiation. Overexpression of EGFR stimulates cells to proliferate. Excessive EGFR...
Induced Pluripotent Stem Cells
Somatic...
Targeted Cancer Therapies
There are several types of targeted therapies against...
Inhibition of Cdk Activity
mTOR Signaling and Cancer Progression
The mTOR pathway or the...