Evidence map›Paper›PMID 32296646›Full record

ReviewFrontiers in oncology2020

Metabolic Reprogramming in Triple-Negative Breast Cancer.

Xiangyu Sun, Mozhi Wang, Mengshen Wang, Xueting Yu, Jingyi Guo, Tie Sun, Xinyan Li, Litong Yao, Haoran Dong, Yingying Xu

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 141 papers.

0numbers the graph read from it
0cells of the map it votes in
141citing papers in PubMed
10.5field-weighted citation impact, top 1% 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

141 citing papers in PubMed, 233 citations in OpenAlex.

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  12. Lactate, a Spearhead of Cancer Aggressiveness: Metabolic Reprogramming, Immune Suppression, and Metastatic Progression.Medical principles and practice : international journal of the Kuwait University, Health Science Centre · 2026
    Review
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  16. Cancer biology & therapy · 2025
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81 more citing papers are in PubMed but not listed here.

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 1 institution in 1 country.

Xiangyu SunDepartment of Breast Surgery, The First Affiliated Hospital of China Medical University, Shenyang, China.
Mozhi WangDepartment of Breast Surgery, The First Affiliated Hospital of China Medical University, Shenyang, China.
Mengshen WangDepartment of Breast Surgery, The First Affiliated Hospital of China Medical University, Shenyang, China.
Xueting YuDepartment of Breast Surgery, The First Affiliated Hospital of China Medical University, Shenyang, China.
Jingyi GuoDepartment of Breast Surgery, The First Affiliated Hospital of China Medical University, Shenyang, China.
Tie SunDepartment of Breast Surgery, The First Affiliated Hospital of China Medical University, Shenyang, China.
Xinyan LiDepartment of Breast Surgery, The First Affiliated Hospital of China Medical University, Shenyang, China.
Litong YaoDepartment of Breast Surgery, The First Affiliated Hospital of China Medical University, Shenyang, China.
Haoran DongDepartment of Breast Surgery, The First Affiliated Hospital of China Medical University, Shenyang, China.
Yingying XuDepartment of Breast Surgery, The First Affiliated Hospital of China Medical University, Shenyang, China.
China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolic reprogramming is an emerging hallmark of cancer cells, in which cancer cells exhibit distinct metabolic phenotypes to fuel their proliferation and progression. The significant advancements made in the area of metabolic reprogramming make possible new strategies for overcoming malignant cancer, including triple-negative breast cancer. Triple-negative breast cancer (TNBC) is associated with high histologic grade, aggressive phenotype, and poor prognosis. Even though triple-negative breast cancer patients benefit from standard chemotherapy, they still face high recurrence rates and are more likely to develop resistance to chemotherapeutic drugs. Therefore, there is an urgent need to explore vulnerabilities of triple-negative breast cancer and develop novel therapeutic drugs to improve clinical outcomes for triple-negative breast cancer patients. Metabolic reprogramming may provide promising therapeutic targets for the treatment of triple-negative breast cancer. In this paper, we primarily discuss how triple-negative breast cancer cells reprogram their metabolic phenotype and that of stromal cells in the microenvironment to survive under nutrient-poor conditions. Considering that metastasis and chemoresistance are the main contributors to mortality in triple-negative breast cancer patients, we also focus on the role of metabolic adaption in mediating metastasis and chemoresistance of triple-negative breast cancer tumors.

Indexed as

glycolysismetabolic networks and pathwaysneoplasm metastasistriple negative breast neoplasmstumor microenvironment

Identifiers

PMID32296646
PMCPMC7136496
OpenAlexW3013544658

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.