The ubiquitin ligase RNF2 stabilizes ERα and modulates breast cancer progression
Open accessAbstract
Estrogen receptor α (ERα) is the most common clinical marker used for breast cancer prognosis and the classification of breast cancer subtypes. Clinically, patients with estrogen receptor-positive breast cancer can receive endocrine therapy. However, resistance to endocrine therapy has become an urgent clinical problem. A large number of previous studies have proven that posttranslational modification of the estrogen receptor is significantly related to endocrine therapy resistance. RNF2 is a member of the RING finger protein family that functions as an E3 ubiquitin ligase. Several studies have clarified that RNF2 is a critical regulator of ERα transcriptional regulation. In our current study, we identified RNF2 as an important posttranslational modification regulator of the estrogen receptor. RNF2 depletion inhibited breast cancer cell progression and ERα signaling activity. TCGA data analysis indicated that RNF2 was elevated in breast malignancies, while RNF2 depletion could drastically inhibit estrogen response gene expression on a whole-genome scale. TCGA data analysis revealed that RNF2 was positively correlated with ERα target gene expression. Further mechanistic studies showed that RNF2 was mainly localized in the nucleus and associated with ERα. The association increased ERα stability by inhibiting ERα K48-linked polyubiquitination. In conclusion, our study implicates nongenomic regulation by RNF2 on ERα protein stability and suggests that targeting RNF2 could be a promising strategy for breast cancer treatments.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
TRIM56, RNF181, and RNF2 stabilize ERα expression.
“It has been reported that the ubiquitin ligases TRIM56, RNF181, and RNF2 stabilize ERα expression30–32.”
From Harnessing artificial intelligence to identify Bufalin as a molecular glue degrader of estrogen receptor alpha (2025) · cites this paper as [30]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Sung, H., Ferlay, J., Siegel, R. L., Laversanne, M., Soerjomataram, I., Jemal, A., & Bray, F. (2021) · CA: A Cancer Journal for Clinicians · doi:10.3322/caac.21660 · Cited by 108,699 · see citing works
Clinical implications of the intrinsic molecular subtypes of breast cancer
Prat, A., Pineda, E., Adamo, B., Galván, P., Fernández-Martínez, A., Gaba, L., Díez, M., Viladot, M., Arance, A. M., & Muñoz-Mateu, M. (2015) · The Breast · doi:10.1016/j.breast.2015.07.008 · Cited by 1,333 · see citing works
Sequence and Expression of Human Estrogen Receptor Complementary DNA
Greene, G. L., Gilna, P., Waterfield, M. D., BAKER, A. J., Hort, Y., & Shine, J. (1986) · Science · doi:10.1126/science.3753802 · Cited by 1,311 · see citing works
Eskeland, R., Leeb, M., Grimes, G. R., Kress, C., Boyle, S., Sproul, D., Gilbert, N., Fan, Y., Skoultchi, A. I., Wutz, A., et al. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.02.032 · Cited by 553 · see citing works
Patel, H., & Bihani, T. (2017) · Pharmacology and Therapeutics · doi:10.1016/j.pharmthera.2017.12.012 · Cited by 423 · see citing works
Sadeh, R., Zaaroor-Regev, D., Ziv, T., & Ciechanover, A. J. (2006) · Molecular Cell · doi:10.1016/j.molcel.2006.10.022 · Cited by 242 · see citing works
Kim, M. Y., Woo, E. M., Chong, Y. E., Homenko, D. R., & Kraus, W. L. (2006) · Molecular Endocrinology · doi:10.1210/me.2005-0531 · Cited by 227 · see citing works
Tamoxifen: Catalyst for the change to targeted therapy
Jordan, V. C. (2007) · European Journal of Cancer · doi:10.1016/j.ejca.2007.11.002 · Cited by 202 · see citing works
The Role of the Estrogen Pathway in the Tumor Microenvironment
Rothenberger, N. J., Somasundaram, A., & Stabile, L. P. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19020611 · Cited by 193 · see citing works
The folate cycle enzyme MTHFD2 induces cancer immune evasion through PD-L1 up-regulation
Shang, M., Yang, H., Yang, R., Chen, T., Fu, Y., Li, Y., Fang, X.-L., Zhang, K., Jianju, Z., Li, H., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-22173-5 · Cited by 184 · see citing works
Self-citationOverview of the relevance of PI3K pathway in HR-positive breast cancer
Vasan, N., Toska, E., & Scaltriti, M. (2019) · Annals of Oncology · doi:10.1093/annonc/mdz281 · Cited by 166 · see citing works
Phosphorylation of Estrogen Receptor α Blocks Its Acetylation and Regulates Estrogen Sensitivity
Cui, Y., Zhang, M., Pestell, R. G., Curran, E. M., Welshons, W. V., & Fuqua, S. A. W. (2004) · Cancer Research · doi:10.1158/0008-5472.can-04-2126 · Cited by 154 · see citing works
Chan, H. L., Beckedorff, F., Zhang, Y., García‐Huidobro, J., Jiang, H. L., Colaprico, A., Bilbao, D., Figueroa, M. E., LaCava, J., Shiekhattar, R., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-05728-x · Cited by 128 · see citing works
Biological mechanisms and clinical implications of endocrine resistance in breast cancer.
Giuliano, M., Schiff, R., Osborne, C., & Trivedi, M. V. (2011) · Breast · doi:10.1016/s0960-9776(11)70293-4 · Cited by 111 · see citing works
Zhu, J., Zhao, C., Razavirad, A., Zhuang, T., Jonsson, P., Liang, N., Williams, C., Lin, C.-Y., Qiao, Y., Zendehdel, K., et al. (2014) · Oncogene · doi:10.1038/onc.2013.573 · Cited by 99 · see citing works
Regulation of estrogen signaling and breast cancer proliferation by an ubiquitin ligase TRIM56
Xue, M., Zhang, K., Mu, K., Xu, J., Yang, H., Liu, Y., Wang, B., Wang, Z., Li, Z., Kong, Q., et al. (2019) · Oncogenesis · doi:10.1038/s41389-019-0139-x · Cited by 97 · see citing works
Self-citationEJE PRIZE 2016: Mechanisms of oestrogen receptor (ER) gene regulation in breast cancer
Carroll, J. S. (2016) · European Journal of Endocrinology · doi:10.1530/eje-16-0124 · Cited by 91 · see citing works
Su, W., Fang, J., Cheng, F., Liu, C., Zhou, F., & Zhang, J. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1211604110 · Cited by 85 · see citing works
Patterns of Genomic Instability in Breast Cancer
Kalimutho, M., Nones, K., Srihari, S., Duijf, P. H. G., Waddell, N., & Khanna, K. K. (2019) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2019.01.005 · Cited by 85 · see citing works
Barone, I., Iacopetta, D., Covington, K. R., Cui, Y., Tsimelzon, A. I., Beyer, A. R., Andò, S., & Fuqua, S. A. W. (2010) · Oncogene · doi:10.1038/onc.2009.520 · Cited by 68 · see citing works
Knockdown of RNF2 induces apoptosis by regulating MDM2 and p53 stability
Wen, W., Peng, C., Kim, M., Jeong, C. H., Zhu, F., Yao, K., Zykova, T. A., Ma, W., Carper, A., Langfald, A., et al. (2013) · Oncogene · doi:10.1038/onc.2012.605 · Cited by 65 · see citing works
Reddel, R. R., & Sutherland, R. L. (1987) · PubMed · Cited by 62 · see citing works
SMURF1 facilitates estrogen receptor ɑ signaling in breast cancer cells
Yang, H., Yu, N. H., Xu, J., Ding, X., Deng, W., Wu, G., Li, X., Hou, Y., Liu, Z., Zhao, Y., et al. (2018) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-018-0672-z · Cited by 61 · see citing works
Self-citationZhang, Y., Chan, H. L., Garcia-Martinez, L., Karl, D. L., Weich, N., Slingerland, J. M., Verdún, R. E., & Morey, L. (2020) · Science Advances · doi:10.1126/sciadv.aaz7249 · Cited by 52 · see citing works
Swetzig, W. M., Wang, J., & Das, G. M. (2016) · Oncotarget · doi:10.18632/oncotarget.7533 · Cited by 42 · see citing works
The ubiquitin ligase RNF181 stabilizes ERα and modulates breast cancer progression
Zhu, J., Li, X., Su, P., Xue, M., Zang, Y., & Ding, Y. (2020) · Oncogene · doi:10.1038/s41388-020-01464-z · Cited by 39 · see citing works
Self-citationEmerging role of RNF2 in cancer: From bench to bedside
Qi, Y., Chen, B., Hu, S., Qi, S., Li, L., Yang, J., Zhou, H., Yang, C., Chen, L., & Du, J. (2021) · Journal of Cellular Physiology · doi:10.1002/jcp.30260 · Cited by 34 · see citing works
Zhang, Y., Liu, T., Yuan, F., Garcia-Martinez, L., Lee, K. D., Stransky, S., Sidoli, S., Verdún, R. E., Zhang, Y., Wang, Z., et al. (2021) · Nucleic Acids Research · doi:10.1093/nar/gkab723 · Cited by 34 · see citing works
Atypical ubiquitin ligase RNF31: the nuclear factor modulator in breast cancer progression
Zhu, J., Zhuang, T., Yang, H., Li, X., Liu, H., & Wang, H. (2016) · BMC Cancer · doi:10.1186/s12885-016-2575-8 · Cited by 34 · see citing works
Self-citationRole of nuclear and membrane estrogen signaling pathways in the male and female reproductive tract
Cooke, P. S., Mesa, A. M., Sirohi, V. K., & Levin, E. R. (2020) · Differentiation · doi:10.1016/j.diff.2020.11.002 · Cited by 23 · see citing works
Koike, H., Ueno, Y., Naito, T., Shiina, T., Nakata, S., Ouchi, R., Obana, Y., Sekine, K., Zheng, Y., Takebe, T., et al. (2014) · Hepatology · doi:10.1002/hep.27046 · Cited by 19 · see citing works
Wu, J., Wang, H., Li, Q., Guo, Q., Tao, S.-Q., Shen, Y., & Wu, Z. (2019) · Pathology - Research and Practice · doi:10.1016/j.prp.2019.152523 · Cited by 14 · see citing works
Flagged first, then by citations
1 of the 33 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
The ubiquitin–proteasome system in breast cancer
Han, D., Wang, L., Jiang, S., & Yang, Q. (2023) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2023.05.006 · Cited by 107 · see citing works
The Role of Estrogen across Multiple Disease Mechanisms
Xiang, X., Palasuberniam, P., & Pare, R. B. (2024) · Current Issues in Molecular Biology · doi:10.3390/cimb46080483 · Cited by 27 · see citing works
Jiang, S., Liu, K., Jiang, T., Li, H., Wei, X., Wan, X., Zhong, C., Gong, R., Chen, Z., Zou, C., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-62288-7 · Cited by 23 · see citing works
Self-citationWang, D., Zhao, J., Yang, X., Ji, Y., Yu, J., Li, Z., Shi, Y., Guo, J., Zhou, J., Hou, L., et al. (2024) · Journal of Virology · doi:10.1128/jvi.00223-24 · Cited by 4 · see citing works
E3 ubiquitin ligase RNF2 protects polymerase ι from destabilization
Fedorowicz, M., Hałas, A., Macias, M., Śledziewska-Gójska, E., Woodgate, R., & McIntyre, J. (2024) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2024.119743 · Cited by 2 · see citing works
Identification and validation of ubiquitination-related genes for predicting cervical cancer outcome
Jin, G., Fan, X., Liang, X., Dai, H., & Wang, J. (2025) · Frontiers in Genetics · doi:10.3389/fgene.2025.1578075
Identification and characterization of key epigenetic drivers of breast cancer
Araujo, M. G. D. S. (2024) · theses.fr (ABES) · doi:10.70675/de1e1ca7zb3fez4d95za929z354256240e6e
BART-spatial unravels biologically significant transcriptional regulators from spatial omics dataPreprint
Wang, J., Zhang, H., Wang, Z., & Zang, C. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.05.05.723027
Zeng, K., Wang, A.-Q., Sun, H.-M., Wang, C.-Y., Wang, S.-L., Zou, R.-L., Yang, D.-J., Bai, Y., Wang, M.-L., Xu, Y.-Y., et al. (2026) · npj Precision Oncology · doi:10.1038/s41698-026-01568-x
- Authors
- Yuan, L., Li, X., Yang, H., & Li, H.
- Affiliations
- Zhengzhou University (CN)
- Henan Medical University (CN)
- Corresponding author
- Yang, Huijie
- Li, Huixiang
- Venue
- Human Cell
- Published
- 2022-10-21
- Volume
- 36
- Issue
- 1
- Pages
- 353-365
- ISSN
- 0914-7470 (ISSN-L)
- 1749-0774
- PMC
- PMC9813066
- OpenAlex
- W4307026328
- Cited by
- 9
- References
- 33
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 4 · 2023: 1
- FWCI
- 1.06
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Locations
- Human Cell (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- The project was supported by Starting Research Funding from Xinxiang Medical University
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Estrogen and related hormone effects
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ubiquitin and proteasome pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Breast Cancer Treatment Studies
- Keywords
- RNF2, estrogen receptor alpha, E3 ubiquitin ligase, breast cancer, endocrine therapy resistance, protein stability, K48-linked polyubiquitination, post-translational modification, RING finger protein
- MeSH terms
- Breast Neoplasms, Female, Humans, Receptors, Estrogen, Gene Expression Regulation, Neoplastic, Ubiquitin, Ubiquitin-Protein Ligases, Cell Line, Tumor, Estrogen Receptor alpha, Polycomb Repressive Complex 1
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review