Evidence map›Paper›PMID 30513627›Full record

ArticleCancers2018

Genomic Characteristics of Invasive Mucinous Adenocarcinomas of the Lung and Potential Therapeutic Targets of B7-H3.

Takahiro Nakagomi, Taichiro Goto, Yosuke Hirotsu, Daichi Shikata, Yujiro Yokoyama, Rumi Higuchi, Sotaro Otake, Kenji Amemiya, Toshio Oyama, Hitoshi Mochizuki and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.1field-weighted citation impact, top 10% 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

29 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
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  7. Impacts ofMolecular imaging and radionuclide therapy · 2024
    Article
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  11. Review
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  17. Journal of personalized medicine · 2021
    Article
  18. Journal of personalized medicine · 2021
    Article
  19. Article
  20. 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

11 authors at 2 institutions in 1 country.

Takahiro NakagomiLung Cancer and Respiratory Disease Center, Yamanashi Central Hospital, Yamanashi 400-8506, Japan. nakagomi.takahiro@gmail.com.
Taichiro GotoLung Cancer and Respiratory Disease Center, Yamanashi Central Hospital, Yamanashi 400-8506, Japan. taichiro@1997.jukuin.keio.ac.jp.ORCID 0000-0002-2560-3639
Yosuke HirotsuGenome Analysis Center, Yamanashi Central Hospital, Yamanashi 400-8506, Japan. hirotsu-bdyu@ych.pref.yamanashi.jp.ORCID 0000-0002-8002-834X
Daichi ShikataLung Cancer and Respiratory Disease Center, Yamanashi Central Hospital, Yamanashi 400-8506, Japan. shikarupd@yahoo.co.jp.
Yujiro YokoyamaLung Cancer and Respiratory Disease Center, Yamanashi Central Hospital, Yamanashi 400-8506, Japan. dooogooodooo@me.com.
Rumi HiguchiLung Cancer and Respiratory Disease Center, Yamanashi Central Hospital, Yamanashi 400-8506, Japan. r-higuchi1504@ych.pref.yamanashi.jp.
Sotaro OtakeLung Cancer and Respiratory Disease Center, Yamanashi Central Hospital, Yamanashi 400-8506, Japan. ootake-bdcg@ych.pref.yamanashi.jp.
Kenji AmemiyaGenome Analysis Center, Yamanashi Central Hospital, Yamanashi 400-8506, Japan. amemiya-bdcd@ych.pref.yamanashi.jp.
Toshio OyamaDepartment of Pathology, Yamanashi Central Hospital, Yamanashi 400-8506, Japan. t-oyama@ych.pref.yamanashi.jp.
Hitoshi MochizukiGenome Analysis Center, Yamanashi Central Hospital, Yamanashi 400-8506, Japan. h-mochiduki2a@ych.pref.yamanashi.jp.ORCID 0000-0002-1145-0969
Masao OmataGenome Analysis Center, Yamanashi Central Hospital, Yamanashi 400-8506, Japan. m-omata0901@ych.pref.yamanashi.jp.
Yamanashi Prefectural Central Hospital · JPKeio University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pulmonary invasive mucinous adenocarcinoma (IMA) is considered a variant of lung adenocarcinomas based on the current World Health Organization classification of lung tumors. However, the molecular mechanism driving IMA development and progression is not well understood. Thus, we surveyed the genomic characteristics of IMA in association with immune-checkpoint expression to investigate new potential therapeutic strategies. Tumor cells were collected from surgical specimens of primary IMA, and sequenced to survey 53 genes associated with lung cancer. The mutational profiles thus obtained were compared in silico to conventional adenocarcinomas and other histologic carcinomas, thereby establishing the genomic clustering of lung cancers. Immunostaining was also performed to compare expression of programmed death ligand 1 (PD-L1) and B7-H3 in IMA and conventional adenocarcinomas. Mutations in Kirsten rat sarcoma viral oncogene homolog (

Indexed as

clusteringimmunocheckpointinvasive mucinous adenocarcinomalung cancernext-generation sequencing

Identifiers

PMID30513627
PMCPMC6316015
OpenAlexW2902061662

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.