Evidence map›Paper›PMID 25938540›Full record

ArticleOncotarget2015

Overexpression of Id1 in transgenic mice promotes mammary basal stem cell activity and breast tumorigenesis.

Dong-Hui Shin, Ji-Hye Park, Jeong-Yeon Lee, Hee-Young Won, Ki-Seok Jang, Kyueng-Whan Min, Si-Hyong Jang, Jong-Kyu Woo, Seung Hyun Oh, Gu Kong

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

12 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Inhibitor of Differentiation 1 (Id1) in Cancer and Cancer Therapy.International journal of medical sciences · 2020
    Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. 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

10 authors at 2 institutions in 1 country.

Dong-Hui ShinDepartment of Pathology, College of Medicine, Hanyang University, Seoul, Republic of Korea.
Ji-Hye ParkInstitute for Bioengineering and Biopharmaceutical Research (IBBR), Hanyang University, Seoul, Republic of Korea.
Jeong-Yeon LeeInstitute for Bioengineering and Biopharmaceutical Research (IBBR), Hanyang University, Seoul, Republic of Korea.
Hee-Young WonDepartment of Pathology, College of Medicine, Hanyang University, Seoul, Republic of Korea.
Ki-Seok JangDepartment of Pathology, College of Medicine, Hanyang University, Seoul, Republic of Korea.
Kyueng-Whan MinDepartment of Pathology, College of Medicine, Hanyang University, Seoul, Republic of Korea.
Si-Hyong JangDepartment of Pathology, College of Medicine, Hanyang University, Seoul, Republic of Korea.
Jong-Kyu WooCollege of Pharmacy, Gachon University, Incheon, Republic of Korea.
Seung Hyun OhCollege of Pharmacy, Gachon University, Incheon, Republic of Korea.
Gu KongDepartment of Pathology, College of Medicine, Hanyang University, Seoul, Republic of Korea.
Hanyang University · KRGachon University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inhibitor of differentiation/DNA binding (Id)1 is a crucial regulator of mammary development and breast cancer progression. However, its effect on stemness and tumorigenesis in mammary epithelial cells remains undefined. Herein, we demonstrate that Id1 induces mammary tumorigenesis by increasing normal and malignant mammary stem cell (MaSC) activities in transgenic mice. MaSC-enriched basal cell expansion and increased self-renewal and in vivo regenerative capacity of MaSCs are observed in the mammary glands of MMTV-Id1 transgenic mice. Furthermore, MMTV-Id1 mice develop ductal hyperplasia and mammary tumors with highly expressed basal markers. Id1 also increases breast cancer stem cell (CSC) population and activity in human breast cancer lines. Moreover, the effects of Id1 on normal and malignant stem cell activities are mediated by the Wnt/c-Myc pathway. Collectively, these findings provide in vivo genetic evidence of Id1 functions as an oncogene in breast cancer and indicate that Id1 regulates mammary basal stem cells by activating the Wnt/c-Myc pathway, thereby contributing to breast tumor development.

Indexed as

AnimalsBlotting, WesternCell Line, TumorCell Transformation, NeoplasticFemaleFlow CytometryHeterograftsHumansImmunohistochemistryInhibitor of Differentiation Protein 1Mammary Neoplasms, ExperimentalMiceMice, TransgenicNeoplastic Stem CellsOncogenesReverse Transcriptase Polymerase Chain ReactionIdb1 protein, mouseInhibitor of Differentiation Protein 1basal-like breast cancercancer stem cellc-MycId1mammary stem cell

Identifiers

PMID25938540
PMCPMC4627307
OpenAlexW1958971964

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.