Evidence map›Paper›PMID 35493295›Full record

ArticleDisease markers2022

BUBs Are New Biomarkers of Promoting Tumorigenesis and Affecting Prognosis in Breast Cancer.

Shunan Wang, Xinyu Liu, Meng Yang, Dongqi Yuan, Kui Ye, Xin Qu, Xinchao Wang

Open access · hybridAbstract read
In one paragraph

Article in Disease markers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

13 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. 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

7 authors at 2 institutions in 1 country.

Shunan WangDepartment of Thyroid and Breast Surgery, Tianjin Fourth Central Hospital, Tianjin 300140, China.ORCID https://orcid.org/0000-0002-3353-7512
Xinyu LiuDepartment of Thyroid and Breast Surgery, Tianjin Fourth Central Hospital, Tianjin 300140, China.ORCID https://orcid.org/0000-0003-2587-046X
Meng YangDepartment of Thyroid and Breast Surgery, Tianjin Fourth Central Hospital, Tianjin 300140, China.ORCID https://orcid.org/0000-0001-5515-4144
Dongqi YuanThe Fourth Central Clinical School, Tianjin Medical University, Tianjin 300140, China.ORCID https://orcid.org/0000-0002-0490-2146
Kui YeDepartment of Vascular Surgery, Tianjin Fourth Central Hospital, Tianjin 300140, China.ORCID https://orcid.org/0000-0003-0783-2865
Xin QuDepartment of Thyroid and Breast Surgery, Tianjin Fourth Central Hospital, Tianjin 300140, China.ORCID https://orcid.org/0000-0001-6556-3347
Xinchao WangDepartment of Thyroid and Breast Surgery, Tianjin Fourth Central Hospital, Tianjin 300140, China.ORCID https://orcid.org/0000-0003-4428-4351
Tianjin Fourth Central Hospital · CNTianjin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: A tumor occurs because of abnormal cell multiplication caused by many variables like a significant disturbance in the regulation of cell growth and the instability of chromosome mitosis. Budding uninhibited by benzimidazoles 1 (BUB1), BUB1 mitotic checkpoint serine/threonine kinase B (BUB1B), and budding uninhibited by benzimidazoles 3 (BUB3) are key regulators of mitosis, and their abnormal expression is highly correlated with breast cancer (BrCa), sarcoma, hepatic carcinoma, and other malignant tumors. However, the occurrence of BUBs (BUB1, BUB1B, and BUB3) and the development of BrCa have not been systematically explained. Methods: Find out the target gene by looking up literature on PubMed and CNKI. Using the R software, TCGA, GEO, Kaplan-Meier Plotter, TIMER, and other databases, we studied the level of transcription, genetic changes, and physiological functions of BUBs in BrCa patients and their relationship with the origin, development, prognosis, immunity, and drug resistance of BrCa patients. Conclusion: We speculate that BUB1, BUB1B, and BUB3 may be therapeutic targets for BrCa patients and also provide new therapeutic strategies for BrCa treatment.

Indexed as

Breast NeoplasmsBenzimidazolesBiomarkersCarcinogenesisCell Cycle ProteinsCell Transformation, NeoplasticFemaleHumansPoly-ADP-Ribose Binding ProteinsPrognosisProtein Serine-Threonine KinasesBenzimidazolesBiomarkersBUB1B protein, humanBUB1 protein, humanBUB3 protein, humanCell Cycle ProteinsPoly-ADP-Ribose Binding ProteinsProtein Serine-Threonine Kinases

Identifiers

PMID35493295
PMCPMC9053761
OpenAlexW4224254423

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.