Evidence map›Paper›PMID 40762777›Full record

ArticleAnnals of surgical oncology2025

Exploring the Role of CDO1 in Breast Cancer: Insights into Tumor Biology and Therapeutic Potential.

Shiori Fujino, Keishi Yamashita, Riku Okamoto, Shumpei Shibaki, Kanako Naito, Hiroyuki Minoura, Kyonosuke Ikemura, Yu Kuroda, Kota Okuno, Akiko Watanabe and 10 more

Abstract read
PubMed Publisher
In one paragraph

Article in Annals of surgical oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

20 authors.

Shiori FujinoDivision of Advanced Surgical Oncology, Research and Development Center for New Medical Frontiers, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.
Keishi YamashitaDivision of Advanced Surgical Oncology, Research and Development Center for New Medical Frontiers, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan. keishi23@med.kitasato-u.ac.jp.ORCID http://orcid.org/0000-0002-8492-0300
Riku OkamotoDivision of Advanced Surgical Oncology, Research and Development Center for New Medical Frontiers, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.
Shumpei ShibakiDivision of Advanced Surgical Oncology, Research and Development Center for New Medical Frontiers, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.
Kanako NaitoDivision of Advanced Surgical Oncology, Research and Development Center for New Medical Frontiers, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.
Hiroyuki MinouraDivision of Advanced Surgical Oncology, Research and Development Center for New Medical Frontiers, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.
Kyonosuke IkemuraDivision of Advanced Surgical Oncology, Research and Development Center for New Medical Frontiers, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.
Yu KurodaDivision of Advanced Surgical Oncology, Research and Development Center for New Medical Frontiers, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.
Kota OkunoDivision of Advanced Surgical Oncology, Research and Development Center for New Medical Frontiers, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.
Akiko WatanabeDivision of Advanced Surgical Oncology, Research and Development Center for New Medical Frontiers, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.
Keiko OkiDivision of Advanced Surgical Oncology, Research and Development Center for New Medical Frontiers, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.
Mikiko KidachiDivision of Advanced Surgical Oncology, Research and Development Center for New Medical Frontiers, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.
Yusuke NieDivision of Advanced Surgical Oncology, Research and Development Center for New Medical Frontiers, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.
Takaaki TokitoDepartment of Breast and Thyroid Surgery, Kitasato University School of Medicine, Sagamihara, Japan.
Mariko KikuchiDepartment of Breast and Thyroid Surgery, Kitasato University School of Medicine, Sagamihara, Japan.
Hiroshi KatoDepartment of Breast and Thyroid Surgery, Kitasato University School of Medicine, Sagamihara, Japan.
Takeshi NaitohDepartment of Lower Gastrointestinal Surgery, Kitasato University School of Medicine, Sagamihara, Japan.
Naoki HikiDepartment of Upper Gastrointestinal Surgery, Kitasato University School of Medicine, Sagamihara, Japan.
Yusuke KumamotoDepartment of General-Pediatric-Hepatobiliary Pancreatic Surgery, Kitasato University School of Medicine, Sagamihara, Japan.
Takafumi SangaiDepartment of Breast and Thyroid Surgery, Kitasato University School of Medicine, Sagamihara, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBreast cancer (BC) is a heterogeneous disease with variable prognosis, highlighting the need for novel biomarkers and therapeutic targets. This study investigates the role of the CDO1 gene, which encodes cysteine dioxygenase 1, in BC progression and its potential impact on patient outcomes. MATERIALS AND

methodsWe performed stable transfection of CDO1 in the MDA-MB231 triple negative BC (TNBC) cell line, followed by analysis of gene expression profiles using microarray technology.

resultsCDO1 is significantly upregulated in transfected cells, leading to the induction of several tumor suppressor genes, including DEFB1, HOPX, and FRMD3. Correlation analysis in clinical BC samples revealed significant associations between CDO1 and other key genes, including SLC1A7 and KITLG, underscoring its relevance in tumor biology. Functional assays demonstrated that CDO1 expression is associated with increased apoptosis and reduced cell viability, suggesting a protective role against tumor progression. Additionally, we observed alterations in oncogenic pathways related to extracellular matrix and protease (SGRN and ADAMTS1), indicating that CDO1 may alleviate metastatic potential putatively via stromal reprogramming.

conclusionsOur findings establish CDO1 as a significant modulator of BC behavior and highlight its potential as a biomarker for prognosis. Further research is warranted to elucidate the underlying mechanisms and explore the therapeutic implications of targeting CDO1 in TNBC.

Indexed as

Breast cancerCDO1Triple negative type

Identifiers

What Socratic holds

Textmetadata
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.