Evidence map›Paper›PMID 36009455›Full record

ArticleBiomedicines2022

Cholesterol Synthesis Is Important for Breast Cancer Cell Tumor Sphere Formation and Invasion.

Hee Yeon Kim, Sung Jin Bae, Ji-Woong Choi, Suji Han, Seung-Hyun Bae, Jae-Ho Cheong, Hyonchol Jang

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 9% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. NONO Maintains SREBP-Regulated Cholesterol Biosynthesis via RNA Binding in Neuroblastoma.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Article
  13. The Effect of Cholesterol in MCF7 Human Breast Cancer Cells.International journal of molecular sciences · 2023
    Article
  14. Article
  15. Review
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

7 authors at 3 institutions in 1 country.

Hee Yeon KimAnticancer Resistance Branch, Division of Rare and Refractory Cancer, National Cancer Center, Research Institute, Goyang 10408, Korea.
Sung Jin BaeAnticancer Resistance Branch, Division of Rare and Refractory Cancer, National Cancer Center, Research Institute, Goyang 10408, Korea.
Ji-Woong ChoiWide River Institute of Immunology, Seoul National University, Hongcheon 25159, Korea.
Suji HanAnticancer Resistance Branch, Division of Rare and Refractory Cancer, National Cancer Center, Research Institute, Goyang 10408, Korea.ORCID 0000-0002-5460-7786
Seung-Hyun BaeAnticancer Resistance Branch, Division of Rare and Refractory Cancer, National Cancer Center, Research Institute, Goyang 10408, Korea.ORCID 0000-0002-6593-0036
Jae-Ho CheongDepartment of Biochemistry and Molecular Biology, Yonsei University College of Medicine, Seoul 03722, Korea.
Hyonchol JangAnticancer Resistance Branch, Division of Rare and Refractory Cancer, National Cancer Center, Research Institute, Goyang 10408, Korea.ORCID 0000-0003-1436-457X
National Cancer Center · KRYonsei University · KRSeoul National University · KR

Funding

National Cancer Center 2110022National Cancer Center 2210350National Research Foundation of Korea 2021R1F1A1060602National Research Foundation of Korea 2022R1A2C2009720
6 · The paper itself

Abstract

Breast cancer has a high risk of recurrence and distant metastasis after remission. Controlling distant metastasis is important for reducing breast cancer mortality, but accomplishing this goal remains elusive. In this study, we investigated the molecular pathways underlying metastasis using cells that mimic the breast cancer distant metastasis process. HCC1143 breast cancer cells were cultured under two-dimensional (2D)-adherent, tumor sphere (TS), and reattached (ReA) culture conditions to mimic primary tumors, circulating tumor cells, and metastasized tumors, respectively. ReA cells demonstrated increased TS formation and enhanced invasion capacity compared to the original 2D-cultured parental cells. In addition, ReA cells had a higher frequency of ESA

Indexed as

breast cancercholesterolinvasionmalignancytumor sphere

Identifiers

PMID36009455
PMCPMC9405659
OpenAlexW4290465906

What Socratic 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 Socratic graph.