Evidence map›Paper›PMID 30128019›Full record

ArticleOncology letters2018

Dissecting the expression landscape of mitochondrial genes in lung squamous cell carcinoma and lung adenocarcinoma.

Nan Li, Jing Zhao, Yibing Ma, Bhaskar Roy, Ren Liu, Karsten Kristiansen, Qiang Gao

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2018. 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
0.3field-weighted citation impact, top 43% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Mitochondria transcription and cancer.Cell death discovery · 2024
    Review
  2. Article
  3. Functional Role of Mitochondrial DNA in Cancer Progression.International journal of molecular sciences · 2022
    Review
  4. Mitochondrial DNA variation and cancer.Nature reviews. Cancer · 2021
    Review
  5. 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

7 authors at 4 institutions in 1 country.

Nan LiLaboratory of Molecular Medicine, Medical College, Eastern Liaoning University, Dandong, Liaoning 118003, P.R. China.
Jing ZhaoBGI Genomics, BGI-Shenzhen, Yantian, Shenzhen, Guangdong 518083, P.R. China.
Yibing MaDepartment of Pathology, Dandong Central Hospital, Dandong, Liaoning 118001, P.R. China.
Bhaskar RoyBGI Genomics, BGI-Shenzhen, Yantian, Shenzhen, Guangdong 518083, P.R. China.
Ren LiuDepartment of Endocrinology, The First Affiliated Hospital of Shenzhen University, Shenzhen University, Shenzhen, Guangdong 518035, P.R. China.
Karsten KristiansenBGI Genomics, BGI-Shenzhen, Yantian, Shenzhen, Guangdong 518083, P.R. China.
Qiang GaoBGI Genomics, BGI-Shenzhen, Yantian, Shenzhen, Guangdong 518083, P.R. China.
BGI Group (China) · CNBGI GenomicsEastern Liaoning University · CNShenzhen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung squamous cell carcinoma (LUSC) and lung adenocarcinoma (LUAD) are the two major subtypes of lung cancer. To explore mitochondrial respiratory gene expression profiles in LUSC and LUAD, RNA sequencing data from The Cancer Genome Atlas was used for comprehensive analyses to establish the molecular characteristics of LUSC and LUAD. To elucidate expression profiles, subtypes were defined using unsupervised clustering of mitochondrial gene expression data. Differences in nuclear gene expression levels, signaling pathways and tumor microenvironments between subtypes were investigated. The analysis revealed that mitochondrial respiratory genes were generally expressed at lower levels in tumor tissues compared with matched control tissues. The expression of mitochondrially encoded NADH dehydrogenase 5 or 6 was associated with tumor progression in LUAD and LUSC. Patients were clustered into three subgroups based on the expression profile of 13 mitochondrial protein-encoding genes, and patients in Cluster 3 exhibited poor survival rates compared with patients from Cluster 1. Furthermore, this association was also observed in another independent data set. Further analyses of the expression of nuclear-encoded genes in the three clusters revealed the enrichment of several cancer-associated signaling pathways in Cluster 3, particularly the apoptotic signaling pathway, suggesting a potential association between the decreased expression of mitochondrial DNA genes and increased tumor aggressiveness. Furthermore, the analyses of immune cell compositions in the tumor microenvironment detected a significant increase in the proportion of CD4

Indexed as

immunotherapylung adenocarcinomalung cancerlung squamous cell carcinomamitochondrial DNARNA expression

Identifiers

PMID30128019
PMCPMC6096099
OpenAlexW2864138999

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.