Evidence map›Paper›PMID 36555470›Full record

ReviewInternational journal of molecular sciences2022

Application of Metabolic Reprogramming to Cancer Imaging and Diagnosis.

Yi-Fang Yang, Chien-Hsiu Li, Huei-Yu Cai, Bo-Syuan Lin, Cheorl-Ho Kim, Yu-Chan Chang

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 41% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Intermittent fasting enhances cancer therapyWorld journal of clinical oncology · 2026
    Review
  3. Review
  4. Article
  5. Progress of Section "Biochemistry" in 2022.International journal of molecular sciences · 2023
    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

6 authors at 4 institutions in 2 countries.

Yi-Fang YangDepartment of Medical Education and Research, Kaohsiung Veterans General Hospital, Kaohsiung 81362, Taiwan.ORCID 0000-0001-7425-3156
Chien-Hsiu LiGenomics Research Center, Academia Sinica, Taipei 115, Taiwan.ORCID 0000-0002-4648-3744
Huei-Yu CaiDepartment of Biomedicine Imaging and Radiological Science, National Yang Ming Chiao Tung University, Taipei 11121, Taiwan.
Bo-Syuan LinDepartment of Biomedicine Imaging and Radiological Science, National Yang Ming Chiao Tung University, Taipei 11121, Taiwan.ORCID 0000-0001-7070-7667
Cheorl-Ho KimDepartment of Biological Sciences, College of Science, Sungkyunkwan University, Seoburo 2066, Suwon 16419, Republic of Korea.ORCID 0000-0002-6323-0714
Yu-Chan ChangDepartment of Biomedicine Imaging and Radiological Science, National Yang Ming Chiao Tung University, Taipei 11121, Taiwan.ORCID 0000-0003-0474-9935
National Yang Ming Chiao Tung University · TWGenomics Research Center, Academia Sinica · TWKaohsiung Veterans General Hospital · TWSamsung (South Korea) · KR

Funding

111 Yen Tjing Ling Medical Foundation CI-111-9Veterans General Hospitals and University System of Taiwan Joint Research Program VGHUST111-G3-3-1Veterans General Hospitals and University System of Taiwan Joint Research Program VGHUST111-G3-3-2
6 · The paper itself

Abstract

Cellular metabolism governs the signaling that supports physiological mechanisms and homeostasis in an individual, including neuronal transmission, wound healing, and circadian clock manipulation. Various factors have been linked to abnormal metabolic reprogramming, including gene mutations, epigenetic modifications, altered protein epitopes, and their involvement in the development of disease, including cancer. The presence of multiple distinct hallmarks and the resulting cellular reprogramming process have gradually revealed that these metabolism-related molecules may be able to be used to track or prevent the progression of cancer. Consequently, translational medicines have been developed using metabolic substrates, precursors, and other products depending on their biochemical mechanism of action. It is important to note that these metabolic analogs can also be used for imaging and therapeutic purposes in addition to competing for metabolic functions. In particular, due to their isotopic labeling, these compounds may also be used to localize and visualize tumor cells after uptake. In this review, the current development status, applicability, and limitations of compounds targeting metabolic reprogramming are described, as well as the imaging platforms that are most suitable for each compound and the types of cancer to which they are most appropriate.

Indexed as

Circadian ClocksNeoplasmsCellular ReprogrammingHomeostasisHumansSignal Transductioncancer metabolismcellular uptakemetabolic reprogrammingmolecular imaging

Identifiers

PMID36555470
PMCPMC9782057
OpenAlexW4311480251

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.