Evidence map›Paper›PMID 35008399›Full record

ReviewCancers2022

Contribution of LAT1-4F2hc in Urological Cancers via Toll-like Receptor and Other Vital Pathways.

Xue Zhao, Shinichi Sakamoto, Maihulan Maimaiti, Naohiko Anzai, Tomohiko Ichikawa

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Comprehensive Characterization of LAT1 Cholesterol-Binding Sites.Journal of chemical theory and computation · 2024
    Article
  4. mCell biology and toxicology · 2024
    Article
  5. Article
  6. Review
  7. 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

5 authors at 1 institution in 2 countries.

Xue ZhaoDepartment of Urology, Chiba University Graduate School of Medicine, Chiba 260-8670, Japan.
Shinichi SakamotoDepartment of Urology, Chiba University Graduate School of Medicine, Chiba 260-8670, Japan.ORCID 0000-0002-7508-7521
Maihulan MaimaitiDepartment of Tumor Pathology, Chiba University Graduate School of Medicine, Chiba 260-8670, Japan.ORCID 0000-0002-3364-1248
Naohiko AnzaiDepartment of Pharmacology, Chiba University Graduate School of Medicine, Chiba 260-8670, Japan.ORCID 0000-0003-0605-0458
Tomohiko IchikawaDepartment of Urology, Chiba University Graduate School of Medicine, Chiba 260-8670, Japan.
Chiba University · JP

Funding

Japan China Sasakawa Medical Fellowship year 2021Japan Society for the Promotion of Science 20H03813 to TI, 20K09555 to SS, and 21H03065 to NA
6 · The paper itself

Abstract

Tumor cells are known for their ability to proliferate. Nutrients are essential for rapidly growing tumor cells. In particular, essential amino acids are essential for tumor cell growth. Tumor cell growth nutrition requires the regulation of membrane transport proteins. Nutritional processes require amino acid uptake across the cell membrane. Leucine, one of the essential amino acids, has recently been found to be closely associated with cancer, which activate mTOR signaling pathway. The transport of leucine into cells requires an L-type amino acid transporter protein 1, LAT1 (SLC7A5), which requires the 4F2 cell surface antigen heavy chain (4F2hc, SLC3A2) to form a heterodimeric amino acid transporter protein complex. Recent evidence identified 4F2hc as a specific downstream target of the androgen receptor splice variant 7 (AR-V7). We stressed the importance of the LAT1-4F2hc complex as a diagnostic and therapeutic target in urological cancers in this review, which covered the recent achievements in research on the involvement of the LAT1-4F2hc complex in urinary system tumors. In addition, JPH203, which is a selective LAT1 inhibitor, has shown excellent inhibitory effects on the proliferation in a variety of tumor cells. The current phase I clinical trials of JPH203 in patients with biliary tract cancer have also achieved good results, which is the future research direction for LAT1 targeted therapy drugs.

Indexed as

4F2 cell-surface antigen heavy chain (4F2hc, SLC3A2)diagnosisL-type amino acid transporter 1 (LAT1, SLC7A)targeted therapyurinary system tumors

Identifiers

PMID35008399
PMCPMC8750950
OpenAlexW4206594139

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.