Evidence map›Paper›PMID 40057746›Full record

ArticleRespiratory research2025

CPHNet: a novel pipeline for anti-HAPE drug screening via deep learning-based Cell Painting scoring.

De-Zhi Sun, Xi-Ru Yang, Cong-Shu Huang, Zhi-Jie Bai, Pan Shen, Zhe-Xin Ni, Chao-Ji Huang-Fu, Yang-Yi Hu, Ning-Ning Wang, Xiang-Lin Tang and 3 more

Abstract read
In one paragraph

Article in Respiratory research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Integration of microphysiological systems with computational and digital twin modeling for pharmaceutical development: a systematic review.Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques · 2026
    Pooled it
  2. Review
  3. Review
  4. Review
  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

13 authors.

De-Zhi Sun *Department of Pharmaceutical Sciences, Beijing Institute of Radiation Medicine, No. 27, Taiping Road, Haidian District, Beijing, 100850, China.ORCID http://orcid.org/0000-0002-0069-452X
Xi-Ru Yang *Department of Pharmacy, Medical College of Qinghai University, Xining, Qinghai, 810001, China.
Cong-Shu Huang *Traditional Chinese Medicine School, Henan University of Chinese Medicine, Zhengzhou, Henan, 450046, China.
Zhi-Jie BaiDepartment of Pharmaceutical Sciences, Beijing Institute of Radiation Medicine, No. 27, Taiping Road, Haidian District, Beijing, 100850, China.
Pan ShenDepartment of Pharmaceutical Sciences, Beijing Institute of Radiation Medicine, No. 27, Taiping Road, Haidian District, Beijing, 100850, China.
Zhe-Xin NiDepartment of Pharmaceutical Sciences, Beijing Institute of Radiation Medicine, No. 27, Taiping Road, Haidian District, Beijing, 100850, China.
Chao-Ji Huang-FuDepartment of Pharmaceutical Sciences, Beijing Institute of Radiation Medicine, No. 27, Taiping Road, Haidian District, Beijing, 100850, China.
Yang-Yi HuDepartment of Pharmacy, Medical College of Qinghai University, Xining, Qinghai, 810001, China.
Ning-Ning WangDepartment of Pharmaceutical Sciences, Beijing Institute of Radiation Medicine, No. 27, Taiping Road, Haidian District, Beijing, 100850, China.
Xiang-Lin TangDepartment of Pharmaceutical Sciences, Beijing Institute of Radiation Medicine, No. 27, Taiping Road, Haidian District, Beijing, 100850, China.
Yong-Fang LiDepartment of Pharmacy, Medical College of Qinghai University, Xining, Qinghai, 810001, China.
Yue GaoDepartment of Pharmacy, Medical College of Qinghai University, Xining, Qinghai, 810001, China. gaoyue@bmi.ac.cn.ORCID http://orcid.org/0000-0003-1131-5326
Wei ZhouDepartment of Pharmacy, Medical College of Qinghai University, Xining, Qinghai, 810001, China. zhouweisyl802@163.com.ORCID http://orcid.org/0000-0003-0435-7261

Funding

National Natural Science Foundation of China 82405196State Administration of Traditional Chinese Medicine of the People's Republic of China ZYYCXTD-D-202207
6 · The paper itself

Abstract

backgroundHigh altitude pulmonary edema (HAPE) poses a significant medical challenge to individuals ascending rapidly to high altitudes. Hypoxia-induced cellular morphological changes in the alveolar-capillary barrier such as mitochondrial structural alterations and cytoskeletal reorganization, play a crucial role in the pathogenesis of HAPE. These morphological changes are critical in understanding the cellular response to hypoxia and represent potential therapeutic targets. However, there is still a lack of effective and valid drug discovery strategies for anti-HAPE treatments based on these cellular morphological features. This study aims to develop a pipeline that focuses on morphological alterations in Cell Painting images to identify potential therapeutic agents for HAPE interventions.

methodsWe generated over 100,000 full-field Cell Painting images of human alveolar adenocarcinoma basal epithelial cells (A549s) and human pulmonary microvascular endothelial cells (HPMECs) under different hypoxic conditions (1%~5% of oxygen content). These images were then submitted to our newly developed segmentation network (SegNet), which exhibited superior performance than traditional methods, to proceed to subcellular structure detection and segmentation. Subsequently, we created a hypoxia scoring network (HypoNet) using over 200,000 images of subcellular structures from A549s and HPMECs, demonstrating outstanding capacity in identifying cellular hypoxia status.

resultsWe proposed a deep neural network-based drug screening pipeline (CPHNet), which facilitated the identification of two promising natural products, ferulic acid (FA) and resveratrol (RES). Both compounds demonstrated satisfactory anti-HAPE effects in a 3D-alveolus chip model (ex vivo) and a mouse model (in vivo).

conclusionThis work provides a brand-new and effective pipeline for screening anti-HAPE agents by integrating artificial intelligence (AI) tools and Cell Painting, offering a novel perspective for AI-driven phenotypic drug discovery.

Indexed as

Altitude SicknessDeep LearningHypertension, PulmonaryA549 CellsAnimalsDrug Evaluation, PreclinicalHumansMiceArtificial intelligence (AI)Cell paintingDrug discoveryHigh altitude pulmonary edema (HAPE)

Identifiers

PMID40057746
PMCPMC11890554

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.