Evidence map›Paper›PMID 31018951›Full record

Trial reportCancer genomics & proteomics

Transcriptome Alterations in Liver Metastases of Colorectal Cancer After Acquired Resistance to Cetuximab.

Zongcheng Li, Yuling Chen, W U Ren, Shuofeng Hu, Zhaoli Tan, Yan Wang, Yaowen Chen, Jian Zhang, Jiaqi Wu, Tingting Li and 2 more

Abstract readClinical Trial
In one paragraph

Trial report in Cancer genomics & proteomics. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
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

12 authors.

Zongcheng LiCenter for Computational Biology, Beijing Institute of Basic Medical Sciences, Beijing, P.R. China.
Yuling ChenDepartment of GI Oncology, 307 Hospital of PLA, Academy of Military Medical Sciences, Beijing, P.R. China.
W U RenCenter for Computational Biology, Beijing Institute of Basic Medical Sciences, Beijing, P.R. China.
Shuofeng HuCenter for Computational Biology, Beijing Institute of Basic Medical Sciences, Beijing, P.R. China.
Zhaoli TanDepartment of GI Oncology, 307 Hospital of PLA, Academy of Military Medical Sciences, Beijing, P.R. China.
Yan WangDepartment of GI Oncology, 307 Hospital of PLA, Academy of Military Medical Sciences, Beijing, P.R. China.
Yaowen ChenCenter for Computational Biology, Beijing Institute of Basic Medical Sciences, Beijing, P.R. China.
Jian ZhangCenter for Computational Biology, Beijing Institute of Basic Medical Sciences, Beijing, P.R. China.
Jiaqi WuCenter for Computational Biology, Beijing Institute of Basic Medical Sciences, Beijing, P.R. China.
Tingting LiDepartment of Geriatric Gastroenterology, Chinese People's Liberation Army General Hospital, Beijing, P.R. China.
Jianming XuDepartment of GI Oncology, 307 Hospital of PLA, Academy of Military Medical Sciences, Beijing, P.R. China yingxmbio@foxmail.com yingxm@bmi.ac.cn jmxu2003@yahoo.com.
Xiaomin YingCenter for Computational Biology, Beijing Institute of Basic Medical Sciences, Beijing, P.R. China yingxmbio@foxmail.com yingxm@bmi.ac.cn jmxu2003@yahoo.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimCetuximab in combination with chemotherapy is recommended as first-line therapy for metastatic colorectal cancer (mCRC) with wild-type RAS. However, drug resistance to cetuximab exists widely in mCRC and reduces the prognosis of patients. Although some genomic alterations have been demonstrated to drive acquired resistance to cetuximab, the overall compendium of inherent molecular mechanisms is still incomplete. MATERIALS AND

methodsFour liver metastasis biopsies were collected from two mCRC patients who were treated with cetuximab in combination with 5-fluororacil plus leucovorin and oxaliplatin (FOLFOX) regimen.

resultsTranscriptomic analysis revealed global gene expression alterations between paired samples prior to treatment and after acquired resistance. Further bioinformatics analysis discovered differentially expressed protein-coding genes/lncRNAs/miRNAs, potential miRNA-mRNA regulatory networks and lncRNA-mRNA competing endogenous RNA network, which may be potential biomarkers or play roles during the process of acquired resistance to cetuximab.

conclusionOur study contributes to deciphering the molecular mechanisms of acquired resistance to cetuximab.

Indexed as

Drug Resistance, NeoplasmGene Expression Regulation, NeoplasticTranscriptomeAntineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorCetuximabColorectal NeoplasmsFluorouracilFollow-Up StudiesGene Regulatory NetworksHumansLeucovorinLiver NeoplasmsOxaliplatinPrognosisRetrospective StudiesBiomarkers, TumorCetuximabFluorouracilLeucovorinOxaliplatinAcquired resistancecetuximabcolorectal cancerregulatory networkstranscriptome alteration

Identifiers

PMID31018951
PMCPMC6542644

What OpenQuestion holds

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Registered trials

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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.