Evidence map›Paper›PMID 32661241›Full record

ArticleScientific reports2020

Proteomic and transcriptomic profiling identifies mediators of anchorage-independent growth and roles of inhibitor of differentiation proteins in invasive lobular carcinoma.

Nilgun Tasdemir, Kai Ding, Laura Savariau, Kevin M Levine, Tian Du, Ashuvinee Elangovan, Emily A Bossart, Adrian V Lee, Nancy E Davidson, Steffi Oesterreich

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

17 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. E-Cadherin-Mediated Cell-Cell Adhesion and Invasive Lobular Breast Cancer.Advances in experimental medicine and biology · 2025
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. 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 6 institutions in 2 countries.

Nilgun TasdemirWomen's Cancer Research Center, University of Pittsburgh Medical Center (UPMC) Hillman Cancer Center (HCC), Magee-Womens Research Institute, 204 Craft Avenue, Pittsburgh, PA, 15213, USA.
Kai DingWomen's Cancer Research Center, University of Pittsburgh Medical Center (UPMC) Hillman Cancer Center (HCC), Magee-Womens Research Institute, 204 Craft Avenue, Pittsburgh, PA, 15213, USA.
Laura SavariauWomen's Cancer Research Center, University of Pittsburgh Medical Center (UPMC) Hillman Cancer Center (HCC), Magee-Womens Research Institute, 204 Craft Avenue, Pittsburgh, PA, 15213, USA.
Kevin M LevineWomen's Cancer Research Center, University of Pittsburgh Medical Center (UPMC) Hillman Cancer Center (HCC), Magee-Womens Research Institute, 204 Craft Avenue, Pittsburgh, PA, 15213, USA.
Tian DuWomen's Cancer Research Center, University of Pittsburgh Medical Center (UPMC) Hillman Cancer Center (HCC), Magee-Womens Research Institute, 204 Craft Avenue, Pittsburgh, PA, 15213, USA.
Ashuvinee ElangovanWomen's Cancer Research Center, University of Pittsburgh Medical Center (UPMC) Hillman Cancer Center (HCC), Magee-Womens Research Institute, 204 Craft Avenue, Pittsburgh, PA, 15213, USA.
Emily A BossartWomen's Cancer Research Center, University of Pittsburgh Medical Center (UPMC) Hillman Cancer Center (HCC), Magee-Womens Research Institute, 204 Craft Avenue, Pittsburgh, PA, 15213, USA.
Adrian V LeeWomen's Cancer Research Center, University of Pittsburgh Medical Center (UPMC) Hillman Cancer Center (HCC), Magee-Womens Research Institute, 204 Craft Avenue, Pittsburgh, PA, 15213, USA.
Nancy E DavidsonFred Hutchinson Cancer Center, Seattle, WA, 98109, USA.
Steffi OesterreichWomen's Cancer Research Center, University of Pittsburgh Medical Center (UPMC) Hillman Cancer Center (HCC), Magee-Womens Research Institute, 204 Craft Avenue, Pittsburgh, PA, 15213, USA. oesterreichs@upmc.edu.
Magee-Womens Research Institute · USUniversity of Pittsburgh Medical Center · USUPMC Hillman Cancer Center · USCancer Research Center · USFred Hutch Cancer Center · USTsinghua University · CN

Funding

VECTOR CORE FACILITYP30CA047904 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Jessie Nedrow · 1988 to 2026
$158.0M
Non-canonical FADD signaling as a genetic driver of invasive lobular carcinomaK99CA237736 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI TASDEMIR, NILGUN · 2019 to 2020
$256k
Combination FGFR4 and ER-Targeted Therapy for Invasive Lobular CarcinomaF30CA203154 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LEVINE, KEVIN MAX · 2017 to 2020
$170k
Targeting the EMT-like Phenotype in Invasive Lobular CarcinomaF31CA203055 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BOSSART, EMILY ANN · 2016 to 2017
$84k
NCI NIH HHS F30 CA203154NCI NIH HHS F31 CA203055NCI NIH HHS K99 CA237736NCI NIH HHS P30 CA047904NIH HHS 1F31CA203055-01NIH HHS 5F30CA203154NIH HHS K99CA237736
6 · The paper itself

Abstract

Invasive lobular carcinoma (ILC) is a histological subtype of breast cancer with distinct molecular and clinical features from the more common subtype invasive ductal carcinoma (IDC). ILC cells exhibit anchorage-independent growth in ultra-low attachment (ULA) suspension cultures, which is largely attributed to the loss of E-cadherin. In addition to anoikis resistance, herein we show that human ILC cell lines exhibit enhanced cell proliferation in ULA cultures as compared to IDC cells. Proteomic comparison of ILC and IDC cell lines identified induction of PI3K/Akt and p90-RSK pathways specifically in ULA culture in ILC cells. Further transcriptional profiling uncovered unique upregulation of the inhibitors of differentiation family transcription factors ID1 and ID3 in ILC ULA culture, the knockdown of which diminished the anchorage-independent growth of ILC cell lines through cell cycle arrest. We find that ID1 and ID3 expression is higher in human ILC tumors as compared to IDC, correlated with worse prognosis uniquely in patients with ILC and associated with upregulation of angiogenesis and matrisome-related genes. Altogether, our comprehensive study of anchorage independence in human ILC cell lines provides mechanistic insights and clinical implications for metastatic dissemination of ILC and implicates ID1 and ID3 as novel drivers and therapeutic targets for lobular breast cancer.

Indexed as

ProteomicsAutoantigensBreast NeoplasmsCadherinsCarcinoma, LobularCell DifferentiationFemaleGene Expression Regulation, NeoplasticHumansInhibitor of Differentiation Protein 1Inhibitor of Differentiation ProteinsIntracellular Signaling Peptides and ProteinsMembrane ProteinsMiddle AgedNeoplasm InvasivenessNeoplasm ProteinsAutoantigensCadherinsCIP2A protein, humanID1 protein, humanID3 protein, humanInhibitor of Differentiation Protein 1Inhibitor of Differentiation ProteinsIntracellular Signaling Peptides and ProteinsMembrane ProteinsNeoplasm ProteinsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktRibosomal Protein S6 Kinases, 90-kDaRPS6KA1 protein, human

Identifiers

PMID32661241
PMCPMC7359337
OpenAlexW3041223721

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.