Evidence map›Paper›PMID 30873683›Full record

ReviewCell proliferation2019

Tumour biomarkers-Tracing the molecular function and clinical implication.

Jiahao Lin, Lie Ma, Di Zhang, Jiafeng Gao, Yipeng Jin, Zhihai Han, Degui Lin

Abstract readReview
In one paragraph

Review in Cell proliferation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 2 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

19 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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  17. Quantification of plasma cell-free DNA levels in dogs with various tumors.Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc · 2019
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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

7 authors.

Jiahao LinThe Clinical Department, College of Veterinary Medicine, China Agricultural University, Beijing, China.
Lie MaDepartment of Respiratory Disease, The Navy General Hospital of PLA, Beijing, China.
Di ZhangThe Clinical Department, College of Veterinary Medicine, China Agricultural University, Beijing, China.
Jiafeng GaoThe Clinical Department, College of Veterinary Medicine, China Agricultural University, Beijing, China.ORCID https://orcid.org/0000-0001-7536-7446
Yipeng JinThe Clinical Department, College of Veterinary Medicine, China Agricultural University, Beijing, China.
Zhihai HanDepartment of Respiratory Disease, The Navy General Hospital of PLA, Beijing, China.
Degui LinThe Clinical Department, College of Veterinary Medicine, China Agricultural University, Beijing, China.

Funding

Fundamental Research Funds for the Central Universities 2017QC076National Nature Science Foundation of China 31502108
6 · The paper itself

Abstract

In recent years, with the increase in cancer mortality caused by metastasis, and with the development of individualized and precise medical treatment, early diagnosis with precision becomes the key to decrease the death rate. Since detecting tumour biomarkers in body fluids is the most non-invasive way to identify the status of tumour development, it has been widely investigated for the usage in clinic. These biomarkers include different expression or mutation in microRNAs (miRNAs), circulating tumour DNAs (ctDNAs), proteins, exosomes and circulating tumour cells (CTCs). In the present article, we summarized and discussed some updated research on these biomarkers. We overviewed their biological functions and evaluated their multiple roles in human and small animal clinical treatment, including diagnosis of cancers, classification of cancers, prognostic and predictive values for therapy response, monitors for therapy efficacy, and anti-cancer therapeutics. Biomarkers including different expression or mutation in miRNAs, ctDNAs, proteins, exosomes and CTCs provide more choice for early diagnosis of tumour detection at early stage before metastasis. Combination detection of these tumour biomarkers may provide higher accuracy at the lowest molecule combination number for tumour early detection. Moreover, tumour biomarkers can provide valuable suggestions for clinical anti-cancer treatment and execute monitoring of treatment efficiency.

Indexed as

Biomarkers, TumorAnimalsDNA MethylationDNA, NeoplasmEarly Detection of CancerExosomesHumansMicroRNAsMutationNeoplasm ProteinsNeoplasmsNeoplastic Cells, CirculatingPredictive Value of TestsPrognosisBiomarkers, TumorDNA, NeoplasmMicroRNAsNeoplasm ProteinsCTCsctDNAsexosomesmiRNAsproteinstumour biomarkers

Identifiers

PMID30873683
PMCPMC6536410

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.