Evidence map›Paper›PMID 37047148›Full record

ReviewInternational journal of molecular sciences2023

Contribution of the L-Type Amino Acid Transporter Family in the Diagnosis and Treatment of Prostate Cancer.

Xue Zhao, Shinichi Sakamoto, Jiaxing Wei, Sangjon Pae, Shinpei Saito, Tomokazu Sazuka, Yusuke Imamura, Naohiko Anzai, Tomohiko Ichikawa

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.8field-weighted citation impact, top 11% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

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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

9 authors at 1 institution in 1 country.

Xue ZhaoDepartment of Urology, Chiba University Graduate School of Medicine, Chiba 260-8670, Japan.ORCID 0000-0003-4818-3064
Shinichi SakamotoDepartment of Urology, Chiba University Graduate School of Medicine, Chiba 260-8670, Japan.ORCID 0000-0002-7508-7521
Jiaxing WeiDepartment of Urology, Chiba University Graduate School of Medicine, Chiba 260-8670, Japan.
Sangjon PaeDepartment of Urology, Chiba University Graduate School of Medicine, Chiba 260-8670, Japan.
Shinpei SaitoDepartment of Urology, Chiba University Graduate School of Medicine, Chiba 260-8670, Japan.
Tomokazu SazukaDepartment of Urology, Chiba University Graduate School of Medicine, Chiba 260-8670, Japan.
Yusuke ImamuraDepartment of Urology, Chiba University Graduate School of Medicine, Chiba 260-8670, Japan.
Naohiko AnzaiDepartment of Pharmacology, Chiba University Graduate School of Medicine, Chiba 260-8670, Japan.
Tomohiko IchikawaDepartment of Urology, Chiba University Graduate School of Medicine, Chiba 260-8670, Japan.ORCID 0000-0002-8637-4163
Chiba University · JP

Funding

Grant-in-Aid for Scientific Research (B) 20H03813Grant-in-Aid for Scientific Research (C) 20K09555Japan China Sasakawa Medical Fellowship N/A
6 · The paper itself

Abstract

The L-type amino acid transporter (LAT) family contains four members, LAT1~4, which are important amino acid transporters. They mainly transport specific amino acids through cell membranes, provide nutrients to cells, and are involved in a variety of metabolic pathways. They regulate the mTOR signaling pathway which has been found to be strongly linked to cancer in recent years. However, in the field of prostate cancer (PCa), the LAT family is still in the nascent stage of research, and the importance of LATs in the diagnosis and treatment of prostate cancer is still unknown. Therefore, this article aims to report the role of LATs in prostate cancer and their clinical significance and application. LATs promote the progression of prostate cancer by increasing amino acid uptake, activating the mammalian target of rapamycin (mTOR) pathway and downstream signals, mediating castration-resistance, promoting tumor angiogenesis, and enhancing chemotherapy resistance. The importance of LATs as diagnostic and therapeutic targets for prostate cancer was emphasized and the latest research results were introduced. In addition, we introduced selective LAT1 inhibitors, including JPH203 and OKY034, which showed excellent inhibitory effects on the proliferation of various tumor cells. This is the future direction of amino acid transporter targeting therapy drugs.

Indexed as

Prostatic NeoplasmsAmino AcidsAmino Acid Transport SystemsHumansMaleSignal TransductionTOR Serine-Threonine KinasesAmino AcidsAmino Acid Transport SystemsTOR Serine-Threonine KinasesdiagnosisLAT1LAT3prostate cancertreatment

Identifiers

PMID37047148
PMCPMC10094571
OpenAlexW4360850230

What OpenQuestion holds

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LicenceCC BY
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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.