Evidence map›Paper›PMID 35216622›Full record

ReviewCell & bioscience2022

Unconventional protein post-translational modifications: the helmsmen in breast cancer.

Jiena Liu, Qin Wang, Yujuan Kang, Shouping Xu, Da Pang

Abstract readReview
In one paragraph

Review in Cell & bioscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
–field-weighted citation impact
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

23 citing papers in PubMed.

  1. Article
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  5. Citrullination in tumor immunity and therapy.The Journal of clinical investigation · 2025
    Review
  6. Tumor-expressed GPNMB orchestrates Siglec-9Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  7. Review
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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

5 authors.

Jiena Liu *Department of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, 150040, China.
Qin Wang *Department of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, 150040, China.
Yujuan KangDepartment of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, 150040, China.
Shouping XuDepartment of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, 150040, China. Shoupingxu@hrbmu.edu.cn.
Da PangDepartment of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, 150040, China. pangda@ems.hrbmu.edu.cn.ORCID http://orcid.org/0000-0003-2853-4170

Funding

National Natural Science Foundation of China 82173235
6 · The paper itself

Abstract

Breast cancer is the most prevalent malignant tumor and a leading cause of mortality among females worldwide. The tumorigenesis and progression of breast cancer involve complex pathophysiological processes, which may be mediated by post-translational modifications (PTMs) of proteins, stimulated by various genes and signaling pathways. Studies into PTMs have long been dominated by the investigation of protein phosphorylation and histone epigenetic modifications. However, with great advances in proteomic techniques, several other PTMs, such as acetylation, glycosylation, sumoylation, methylation, ubiquitination, citrullination, and palmitoylation have been confirmed in breast cancer. Nevertheless, the mechanisms, effects, and inhibitors of these unconventional PTMs (particularly, the non-histone modifications other than phosphorylation) received comparatively little attention. Therefore, in this review, we illustrate the functions of these PTMs and highlight their impact on the oncogenesis and progression of breast cancer. Identification of novel potential therapeutic drugs targeting PTMs and development of biological markers for the detection of breast cancer would be significantly valuable for the efficient selection of therapeutic regimens and prediction of disease prognosis in patients with breast cancer.

Indexed as

Breast cancerOncogenesisPost-translational modificationsProteomics

Identifiers

PMID35216622
PMCPMC8881842

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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.