Evidence map›Paper›PMID 33537930›Full record

ArticleIn vitro cellular & developmental biology. Animal2021

Enhanced KRT13 gene expression bestows radiation resistance in squamous cell carcinoma cells.

Tam Quang Nguyen, Atsuko Hamada, Kaori Yamada, Mirai Higaki, Tomoaki Shintani, Yukio Yoshioka, Shigeaki Toratani, Tetsuji Okamoto

Abstract read
PubMed Publisher
In one paragraph

Article in In vitro cellular & developmental biology. Animal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
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  4. Identification ofFrontiers in cell and developmental biology · 2022
    Article
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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

8 authors.

Tam Quang Nguyen *Department of Molecular Oral Medicine and Maxillofacial Surgery, Graduate School of Biomedical and Health Sciences, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima, 734-8553, Japan.
Atsuko Hamada *Oral and Maxillofacial Surgery, Hiroshima University Hospital, Hiroshima, Japan.
Kaori YamadaOral and Maxillofacial Surgery, Hiroshima University Hospital, Hiroshima, Japan.
Mirai HigakiOral and Maxillofacial Surgery, Hiroshima University Hospital, Hiroshima, Japan.
Tomoaki ShintaniOral and Maxillofacial Surgery, Hiroshima University Hospital, Hiroshima, Japan.
Yukio YoshiokaDepartment of Molecular Oral Medicine and Maxillofacial Surgery, Graduate School of Biomedical and Health Sciences, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima, 734-8553, Japan.
Shigeaki TorataniDepartment of Molecular Oral Medicine and Maxillofacial Surgery, Graduate School of Biomedical and Health Sciences, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima, 734-8553, Japan.
Tetsuji OkamotoDepartment of Molecular Oral Medicine and Maxillofacial Surgery, Graduate School of Biomedical and Health Sciences, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima, 734-8553, Japan. tetsuok@hiroshima-u.ac.jp.ORCID http://orcid.org/0000-0001-7392-5547

Funding

Japan Society for the Promotion of Science 18H03000Japan Society for the Promotion of Science 19K191980A
6 · The paper itself

Abstract

Cancer metastasis and recurrence are potentially lethal. A small number of cancer cell groups called cancer stem cells (CSCs) have both stem cell capacity and cancer-forming ability and are reported to play important roles in cancer metastasis and recurrence. These CSCs are considered to be radiation-resistant (RR). Therefore, understanding the biological effects of radiation on squamous cell carcinoma (SCC) cell lines in vitro and in vivo might be worthwhile to circumvent radiation resistance. Currently, there are no reports on the establishment of RR-SCC cells in serum-free defined culture, which mimics biological mechanisms and prevents instability of using serum in the culture medium. We isolated radiation-resistant strains, designated A431-LDR and A431-HDR, from A431 cells derived from vulval SCC and irradiated them with a total dose of 60 Gy at a low-dose rate (2.2 Gy/d) (RM1000) and a high-dose rate (5 Gy/5.75min) in serum-free defined culture. These cells exhibited high sphere-forming and migration ability in vitro and high tumor-forming ability in nude mice xenografts. Overexpression of KRT13 in A431-RR cells might play a role in its radiation-resistant characteristics. These cells might be useful not only to study cancer stem cells but also to study the circumvention of radiation resistance by novel cancer treatment modalities.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsCarcinogenesisCarcinoma, Squamous CellCell Line, TumorCell MovementCell ProliferationCulture Media, Serum-FreeDose-Response Relationship, RadiationFemaleHumansKeratin-13MiceMice, NudeNeoplastic Stem CellsRadiation ToleranceCulture Media, Serum-FreeKeratin-13KRT13 protein, humanRNA, Small InterferingKRT13Radiation-resistant carcinoma cell strainsSerum-free defined culture

Identifiers

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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.