Evidence map›Paper›PMID 40061435›Full record

ArticleBioactive materials2025

Establishing a cryopreserved biobank of living tumor tissues for drug sensitivity testing.

Ping Chen, Jing-Bo Zhou, Xiang-Peng Chu, Yang-Yang Feng, Qi-Bing Zeng, Josh-Haipeng Lei, Ka-Pou Wong, Tai-Ip Chan, Chon-Wa Lam, Wen-Li Zhu and 5 more

Abstract read
In one paragraph

Article in Bioactive materials, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
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

15 authors.

Ping ChenCancer Centre, Faculty of Health Sciences, University of Macau, Macau SAR 999078, China.
Jing-Bo ZhouCancer Centre, Faculty of Health Sciences, University of Macau, Macau SAR 999078, China.
Xiang-Peng ChuCancer Centre, Faculty of Health Sciences, University of Macau, Macau SAR 999078, China.
Yang-Yang FengCancer Centre, Faculty of Health Sciences, University of Macau, Macau SAR 999078, China.
Qi-Bing ZengCancer Centre, Faculty of Health Sciences, University of Macau, Macau SAR 999078, China.
Josh-Haipeng LeiCancer Centre, Faculty of Health Sciences, University of Macau, Macau SAR 999078, China.
Ka-Pou WongCancer Centre, Faculty of Health Sciences, University of Macau, Macau SAR 999078, China.
Tai-Ip ChanKiang Wu Hospital, Macau SAR 999078, China.
Chon-Wa LamKiang Wu Hospital, Macau SAR 999078, China.
Wen-Li ZhuKiang Wu Hospital, Macau SAR 999078, China.
Wai-Kuok ChuKiang Wu Hospital, Macau SAR 999078, China.
Feng HuKiang Wu Hospital, Macau SAR 999078, China.
Guang-Hui LuoKiang Wu Hospital, Macau SAR 999078, China.
Kin-Iong ChanKiang Wu Hospital, Macau SAR 999078, China.
Chu-Xia DengCancer Centre, Faculty of Health Sciences, University of Macau, Macau SAR 999078, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The cryopreservation of cancer tissues to generate frozen libraries is a common practice used worldwide for storing patient samples for later applications. However, frozen samples stored by existing methods cannot be used for initiating living cell cultures, such as patient-derived tumor organoids (PDOs), which offer great potential for personalized treatment. To overcome this challenge, we developed a novel procedure for culturing PDOs using frozen live tumor tissues. We show that tumor specimens stored using this technique maintain their viability and can be successfully used to generate organoids even after long-term freezing, with an impressive success rate of 95.2 %. Importantly, we found that the structural features, tumor marker expression, and drug responses of organoids derived from frozen tissues are similar to those derived from fresh tissues. Moreover, organoids derived from frozen tissues can be routinely passaged and frozen, making them ideal for high-throughput drug screening at any time. Notably, cryopreserved tumor tissues can also be utilized in air-liquid interface (ALI) culture. This method allows for preserving the original tumor microenvironment, making it an invaluable resource for conducting tests on antitumor drug responses, including immune checkpoint inhibitors (ICIs). This innovation has the potential to enable the identification of potentially effective drugs for patients and facilitate the development of novel therapeutic drugs. Thus, we have established protocols for the long-term cryopreservation of cancer tissues to maintain their viability and microenvironment, which are useful for personalized therapy.

Indexed as

Air-liquid interface (ALI) cultureBiobankLiving tumor tissuesPatient-derived organoids (PDOs)Personalized therapy

Identifiers

PMID40061435
PMCPMC11889390

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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.