Evidence map›Paper›PMID 28423597›Full record

ArticleOncotarget2017

HRD1 sensitizes breast cancer cells to Tamoxifen by promoting S100A8 degradation.

YanYang Wang, AiBin Guo, XiuBin Liang, Min Li, Ming Shi, Yan Li, Gareth Jenkins, XiaWen Lin, XueFei Wei, ZhiJun Jia and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 23% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. The crosstalk between ubiquitination and endocrine therapy.Journal of molecular medicine (Berlin, Germany) · 2023
    Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 1 country.

YanYang WangDepartment of Nuclear Medicine, The Affiliated Drum Tower Hospital of Nanjing University, Nanjing, China.
AiBin GuoDepartment of Geriatric Medicine, The Affiliated Drum Tower Hospital of Nanjing University, Nanjing, China.
XiuBin LiangDepartment of Surgical Oncology, The First Affiliated Hospital With Nanjing Medical University, Nanjing, China.
Min LiDepartment of Surgical Oncology, The First Affiliated Hospital With Nanjing Medical University, Nanjing, China.
Ming ShiDepartment of Nuclear Medicine, The Affiliated Drum Tower Hospital of Nanjing University, Nanjing, China.
Yan LiCenter of Pathology and Clinical Laboratory, Sir Run Run Hospital, Nanjing Medical University, Nanjing, China.
Gareth JenkinsInstitute of Advanced Materials, Nanjing University of Post and Telecommunication, Nanjing, China.
XiaWen LinDepartment of Nuclear Medicine, The Affiliated Drum Tower Hospital of Nanjing University, Nanjing, China.
XueFei WeiDepartment of Nuclear Medicine, The Affiliated Drum Tower Hospital of Nanjing University, Nanjing, China.
ZhiJun JiaDepartment of Nuclear Medicine, The Affiliated Drum Tower Hospital of Nanjing University, Nanjing, China.
XueFeng FengDepartment of Nuclear Medicine, The Affiliated Drum Tower Hospital of Nanjing University, Nanjing, China.
DongMing SuCenter of Pathology and Clinical Laboratory, Sir Run Run Hospital, Nanjing Medical University, Nanjing, China.
WanHua GuoDepartment of Nuclear Medicine, The Affiliated Drum Tower Hospital of Nanjing University, Nanjing, China.
Nanjing Drum Tower Hospital · CNNanjing Medical University · CNNanjing University of Posts and Telecommunications · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Estrogen receptor alpha positive (ER+) of breast cancer could develop resistance to antiestrogens including Tamoxifen. Our previous study showed that the E3 ubiquitin ligase HRD1 played an important role in anti-breast cancer. However, its role in chemotherapy resistance hasn't been reported. In this study, we found that HRD1 expression was downregulated in Tamoxifen-resistant breast cancer cell line MCF7/Tam compared to the Tamoxifen sensitive cell line MCF7. Moreover, S100A8 is the direct target of HRD1 by proteome analysis. Our data showed that HRD1 decreased the protein level of S100A8 through ubiquitination while HRD1 was regulated by acetylation of histone. More importantly, HRD1 knockdown significantly increased the cell survival of MCF7 cells to the Tamoxifen treatment. HRD1 overexpression sensitized MCF7/Tam cells to the Tamoxifen treatment in vitro and in vivo. In conclusion, the decrease of HRD1 expression contributed to Tamoxifen resistance in breast cancer.

Indexed as

AcetylationAnimalsBlotting, WesternBreast NeoplasmsCalgranulin ACell SurvivalDrug Resistance, NeoplasmEstrogen AntagonistsFemaleGene Expression Regulation, NeoplasticHistonesHumansMCF-7 CellsMice, NudeMicroscopy, FluorescenceProtein BindingCalgranulin AEstrogen AntagonistsHistonesSYVN1 protein, humanTamoxifenUbiquitin-Protein Ligaseschemotherapy resistanceHRD1S100A8Tamoxifen

Identifiers

PMID28423597
PMCPMC5410327
OpenAlexW2592124065

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.