Evidence map›Paper›PMID 35647127›Full record

ReviewWorld journal of clinical cases2022

Targeting metabolism: A potential strategy for hematological cancer therapy.

Xue Tang, Fen Chen, Li-Chun Xie, Si-Xi Liu, Hui-Rong Mai

Abstract readReview
In one paragraph

Review in World journal of clinical cases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Xue TangDepartment of Hematology and Oncology, Shenzhen Children's Hospital, Shenzhen 518038, Guangdong Province, China.
Fen ChenDepartment of Hematology and Oncology, Shenzhen Children's Hospital, Shenzhen 518038, Guangdong Province, China.
Li-Chun XieDepartment of Hematology and Oncology, Shenzhen Children's Hospital, Shenzhen 518038, Guangdong Province, China.
Si-Xi LiuDepartment of Hematology and Oncology, Shenzhen Children's Hospital, Shenzhen 518038, Guangdong Province, China.
Hui-Rong MaiDepartment of Hematology and Oncology, Shenzhen Children's Hospital, Shenzhen 518038, Guangdong Province, China. maihuirong@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Most hematological cancer-related relapses and deaths are caused by metastasis; thus, the importance of this process as a target of therapy should be considered. Hematological cancer is a type of cancer in which metabolism plays an essential role in progression. Therefore, we are required to block fundamental metastatic processes and develop specific preclinical and clinical strategies against those biomarkers involved in the metabolic regulation of hematological cancer cells, which do not rely on primary tumor responses. To understand progress in this field, we provide a summary of recent developments in the understanding of metabolism in hematological cancer and a general understanding of biomarkers currently used and under investigation for clinical and preclinical applications involving drug development. The signaling pathways involved in cancer cell metabolism are highlighted and shed light on how we could identify novel biomarkers involved in cancer development and treatment. This review provides new insights into biomolecular carriers that could be targeted as anticancer biomarkers.

Indexed as

AnticancerBiomarkerCancerHematological cancerMetabolismMetastasis

Identifiers

PMID35647127
PMCPMC9082716

What Socratic holds

Textmetadata
LicenceCC BY-NC
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.