Evidence map›Paper›PMID 30067437›Full record

ArticleCancer biology & therapy2018

Mutational landscape and clonal diversity of pulmonary adenoid cystic carcinoma.

Min Li, Bing-Rong Zhao, Shi-Qing Liu, Jian An, Peng-Bo Deng, Han Han-Zhang, Jun-Yi Ye, Xin-Ru Mao, Shao-Kun Chuai, Cheng-Ping Hu

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biology & therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Targeted therapy for rare lung cancers: Status, challenges, and prospects.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    Review
  5. Review
  6. Article
  7. Article
  8. Clinicopathologic Features and Prognosis ofFrontiers in oncology · 2020
    Article
  9. Article
  10. TheCancer biology & therapy · 2019
    Article
  11. 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

10 authors at 2 institutions in 1 country.

Min Lia Department of Respiratory Medicine , Xiangya Hospital, Central South University , Changsha , China.ORCID 0000-0002-3578-2239
Bing-Rong Zhaoa Department of Respiratory Medicine , Xiangya Hospital, Central South University , Changsha , China.
Shi-Qing Liua Department of Respiratory Medicine , Xiangya Hospital, Central South University , Changsha , China.
Jian Ana Department of Respiratory Medicine , Xiangya Hospital, Central South University , Changsha , China.
Peng-Bo Denga Department of Respiratory Medicine , Xiangya Hospital, Central South University , Changsha , China.
Han Han-Zhangc Burning Rock Biotech , Guangzhou , China.
Jun-Yi Yec Burning Rock Biotech , Guangzhou , China.
Xin-Ru Maoc Burning Rock Biotech , Guangzhou , China.
Shao-Kun Chuaic Burning Rock Biotech , Guangzhou , China.
Cheng-Ping Hua Department of Respiratory Medicine , Xiangya Hospital, Central South University , Changsha , China.
Central South University · CNBurning Rock Biotech (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pulmonary adenoid cystic carcinoma is a rare and indolent lung malignancy, characterized by a protracted but unpredictable growth behavior. Currently, the treatment of PACC relies on surgery and local radiotherapy. However, treatment options for advanced PACC patients are limited. A larger number of studies demonstrated that advanced PACC patients obtained limited benefit from chemotherapy. Moreover, only a few case reports revealed PACC patients were candidates for target therapy. Therefore, there is an urgent need to develop novel therapies. Due to its rareness, its mutational landscape remains largely elusive. In this study, we performed capture-based ultra-deep sequencing on multiregional surgical specimens obtained from 8 PACC patients using a panel consisting of 295 cancer-related genes. Our data revealed distinctive mutational spectrum of PACC, which differed from non-small cell lung cancer and adenoid cystic carcinomas originated from other anatomical sites. PACC, lacking mutations in a majority of non-small cell lung cancer driver genes, has frequent mutations in genes participating in chromatin remodeling and NOTCH signaling pathway. We also elucidated spatial intra-tumoral heterogeneity, which varied among cases. Most mutations in chromatin remodelers were subclonal. Collectively, our findings elucidated molecular signature associated with PACC and highlighted the potential for epigenetic therapy in this disease.

Indexed as

Biomarkers, TumorGenetic HeterogeneityMutationAdultCarcinoma, Adenoid CysticChromatin Assembly and DisassemblyClonal EvolutionDNA Mutational AnalysisEpigenesis, GeneticFemaleHumansLung NeoplasmsMaleMiddle AgedNeoplasm StagingReceptors, NotchBiomarkers, TumorReceptors, NotchChinesechromatin remodelingclonal diversityepigenetic therapymutational landscapeNOTCH signalingpulmonary adenoid cystic carcinoma

Identifiers

PMID30067437
PMCPMC6300342
OpenAlexW2886220637

What OpenQuestion holds

Textmetadata
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.