Evidence map›Paper›PMID 40701982›Full record

ArticleOncogenesis2025

Targeting SLC7A5 in lung squamous cell carcinoma: implications for cancer metabolism shift and boron neutron capture therapy resistance.

Yen-Ju Lin, Yu-Cheng Wu, Yu-Jui Liu, Wei-Chen Yeh, Yi-Chen Huang, Shen-Ao Zhang, Alvin Chen, Ming-Yi Zheng, Hong-Ming Liu, Fong-In Chou and 3 more

Abstract read
In one paragraph

Article in Oncogenesis, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

13 authors.

Yen-Ju LinInstitute of Biotechnology, National Tsing Hua University, Hsinchu, Taiwan.
Yu-Cheng WuInstitute of Biotechnology, National Tsing Hua University, Hsinchu, Taiwan.
Yu-Jui LiuInstitute of Biotechnology, National Tsing Hua University, Hsinchu, Taiwan.
Wei-Chen YehInstitute of Biotechnology, National Tsing Hua University, Hsinchu, Taiwan.
Yi-Chen HuangInstitute of Biotechnology, National Tsing Hua University, Hsinchu, Taiwan.
Shen-Ao ZhangInstitute of Biotechnology, National Tsing Hua University, Hsinchu, Taiwan.
Alvin ChenInstitute of Biotechnology, National Tsing Hua University, Hsinchu, Taiwan.
Ming-Yi ZhengInstitute of Biotechnology, National Tsing Hua University, Hsinchu, Taiwan.
Hong-Ming LiuNuclear Science and Technology Development Center, National Tsing Hua University, Hsinchu, Taiwan.
Fong-In ChouNuclear Science and Technology Development Center, National Tsing Hua University, Hsinchu, Taiwan.
Shien-Tung PanDepartment of Pathology, China Medical University Hsinchu Hospital, Hsinchu County, Taiwan.
Min-Yuan Chou *Innovation and Advanced Research Office, Biomedical Technology and Device Research Laboratories, Industrial Technology Research Institute, Hsinchu, Taiwan.
Yu-Ting Chou *Institute of Biotechnology, National Tsing Hua University, Hsinchu, Taiwan. ytchou@life.nthu.edu.tw.ORCID http://orcid.org/0000-0001-9274-8603

Funding

Ministry of Science and Technology, Taiwan (Ministry of Science and Technology of Taiwan) 109-2320-B-007-003-MY3Ministry of Science and Technology, Taiwan (Ministry of Science and Technology of Taiwan) 112-2320-B-007-005
6 · The paper itself

Abstract

Squamous cell carcinoma (SCC) poses a significant global health challenge due to the lack of effective treatments. Boron neutron capture therapy (BNCT), a targeted particle therapy, has shown promising results in various cancers. SLC7A5, a transporter of essential amino acids and boronophenylalanine (BPA) used in BNCT, emerges as a potential therapeutic target. However, its expression across different histological subtypes and the role of SLC7A5 inhibition in developing drug resistance to BPA-BNCT remain poorly understood. Our study reveals elevated SLC7A5 expression in most SCCs, particularly in lung squamous cell carcinoma (LUSC), where it is significantly higher compared to other lung cancer subtypes. Increased SLC7A5 expression and a higher tumor-to-normal (T/N) ratio in LUSC are associated with poor patient prognosis. SLC7A5 knockdown in LUSC cells reduces colony formation and induces apoptosis. RNA-seq analysis of SLC7A5 knockout LUSC cells shows downregulated mTORC1 signaling, reduced expression of other amino acid transporters, and upregulated autophagy genes, indicating a potential cancer metabolic shift. Furthermore, SLC7A5 knockout LUSC cells demonstrate resistance to BPA-BNCT but sensitivity to the autophagy inhibitor chloroquine. Post-BPA-BNCT treatment, surviving wild-type LUSC cells exhibit reduced SLC7A5 levels and increased sensitivity to chloroquine, highlighting a vulnerability in BPA-BNCT-resistant cells. Our findings elucidate the interplay between SLC7A5, mTOR signaling, and autophagy pathways, providing insights into potential strategies to overcome drug resistance in BPA-BNCT therapy.

Identifiers

PMID40701982
PMCPMC12287270

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Registered trials

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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.