Evidence map›Paper›PMID 36012461›Full record

ReviewInternational journal of molecular sciences2022

Mouse Models for Immune Checkpoint Blockade Therapeutic Research in Oral Cancer.

Wei-Chiao Chiu, Da-Liang Ou, Ching-Ting Tan

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. 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
1.8field-weighted citation impact, top 13% 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, 18 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

3 authors at 2 institutions in 1 country.

Wei-Chiao ChiuDepartment of Medical Research, Fu-Jen Catholic University Hospital, Fu-Jen Catholic University, New Taipei City 24352, Taiwan.
Da-Liang OuGraduate Institute of Oncology, College of Medicine, National Taiwan University, Taipei City 10051, Taiwan.ORCID 0000-0002-8368-1141
Ching-Ting TanDepartment of Otolaryngology, National Taiwan University Hospital, Taipei City 100225, Taiwan.
National Taiwan University · TWFu Jen Catholic University · TW

Funding

Ministry of Education, Taiwan NTU-109L901403, NTU- 110L901404Ministry of Science and Technology, Taiwan MOST 109-2634-F-002-043, 109-2314-B-002 -229 -MY3, MOST 109-2314-B-002-057-MY3, MOST 110-2634-F-002-044National Health Research Institutes, Taiwan NHRI-111-B06National Taiwan University YongLin Chair Grant S-01National Taiwan University Hospital UN109-051, MS251
6 · The paper itself

Abstract

The most prevalent oral cancer globally is oral squamous cell carcinoma (OSCC). The invasion of adjacent bones and the metastasis to regional lymph nodes often lead to poor prognoses and shortened survival times in patients with OSCC. Encouraging immunotherapeutic responses have been seen with immune checkpoint inhibitors (ICIs); however, these positive responses to monotherapy have been limited to a small subset of patients. Therefore, it is urgent that further investigations into optimizing immunotherapies are conducted. Areas of research include identifying novel immune checkpoints and targets and tailoring treatment programs to meet the needs of individual patients. Furthermore, the advancement of combination therapies against OSCC is also critical. Thus, additional studies are needed to ensure clinical trials are successful. Mice models are advantageous in immunotherapy research with several advantages, such as relatively low costs and high tumor growth success rate. This review paper divided methods for establishing OSCC mouse models into four categories: syngeneic tumor models, chemical carcinogen induction, genetically engineered mouse, and humanized mouse. Each method has advantages and disadvantages that influence its application in OSCC research. This review comprehensively surveys the literature and summarizes the current mouse models used in immunotherapy, their advantages and disadvantages, and details relating to the cell lines for oral cancer growth. This review aims to present evidence and considerations for choosing a suitable model establishment method to investigate the early diagnosis, clinical treatment, and related pathogenesis of OSCC.

Indexed as

Carcinoma, Squamous CellHead and Neck NeoplasmsMouth NeoplasmsAnimalsDisease Models, AnimalImmune Checkpoint InhibitorsMiceSquamous Cell Carcinoma of Head and NeckTherapeutic Human ExperimentationImmune Checkpoint Inhibitorschemical carcinogen inductiongenetically engineered mousehumanized mouseimmune checkpoint inhibitorsoral squamous cell carcinomasyngeneic tumor modelstumor microenvironment

Identifiers

PMID36012461
PMCPMC9409124
OpenAlexW4292295081

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.