Evidence map›Paper›PMID 30563990›Full record

ArticleBritish journal of cancer2019

Alterations in serum amino-acid profile in the progression of colorectal cancer: associations with systemic inflammation, tumour stage and patient survival.

Päivi Sirniö, Juha P Väyrynen, Kai Klintrup, Jyrki Mäkelä, Toni Karhu, Karl-Heinz Herzig, Ilkka Minkkinen, Markus J Mäkinen, Tuomo J Karttunen, Anne Tuomisto

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 9% 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

58 citing papers in PubMed, 1 synthesis or guideline pooled it, 102 citations in OpenAlex.

  1. Pooled it
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  6. Cancer cachexia: molecular basis and therapeutic advances.Signal transduction and targeted therapy · 2026
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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

10 authors at 3 institutions in 2 countries.

Päivi SirniöCancer and Translational Medicine Research Unit, University of Oulu, POB 5000, 90014, Oulu, Finland.
Juha P VäyrynenCancer and Translational Medicine Research Unit, University of Oulu, POB 5000, 90014, Oulu, Finland.ORCID http://orcid.org/0000-0002-8683-2996
Kai KlintrupOulu University Hospital and Medical Research Center Oulu, POB 21, 90029, Oulu, Finland.
Jyrki MäkeläOulu University Hospital and Medical Research Center Oulu, POB 21, 90029, Oulu, Finland.
Toni KarhuDepartment of Physiology, Research Unit of Biomedicine and Biocenter Oulu, University of Oulu, POB 5000, 90014, Oulu, Finland.
Karl-Heinz HerzigOulu University Hospital and Medical Research Center Oulu, POB 21, 90029, Oulu, Finland.
Ilkka MinkkinenCancer and Translational Medicine Research Unit, University of Oulu, POB 5000, 90014, Oulu, Finland.
Markus J MäkinenCancer and Translational Medicine Research Unit, University of Oulu, POB 5000, 90014, Oulu, Finland.
Tuomo J KarttunenCancer and Translational Medicine Research Unit, University of Oulu, POB 5000, 90014, Oulu, Finland.
Anne TuomistoCancer and Translational Medicine Research Unit, University of Oulu, POB 5000, 90014, Oulu, Finland. anne.tuomisto@oulu.fi.ORCID http://orcid.org/0000-0002-9949-1887
Oulu University Hospital · FIPoznan University of Medical Sciences · PLUniversity of Oulu · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCancer cachexia is a complex wasting syndrome affecting patients with advanced cancer, with systemic inflammation as a key component in pathogenesis. Protein degradation and release of amino acids (AAs) in skeletal muscle are stimulated in cachexia. Here, we define factors contributing to serum AA levels in colorectal cancer (CRC).

methodsSerum levels of nine AAs were characterised in 336 CRC patients and their relationships with 20 markers of systemic inflammatory reaction, clinicopathological features of cancers and patient survival were analysed.

resultsLow serum glutamine and histidine levels and high phenylalanine levels associated with indicators of systemic inflammation, including high modified Glasgow Prognostic Score, high blood neutrophil/lymphocyte ratio and high serum levels of CRP, IL-6 and IL-8. Low levels of serum glutamine, histidine, alanine and high glycine levels also associated with advanced cancer stage and with poor cancer-specific survival in univariate analysis.

conclusionsIn CRC, serum AA levels are associated with systemic inflammation and disease stage. These findings may reflect muscle catabolism induced by systemic inflammation in CRC.

Indexed as

AgedAmino AcidsBiomarkers, TumorColorectal NeoplasmsCytokinesDisease-Free SurvivalDisease ProgressionFemaleHumansInflammationLymphocytesMaleMiddle AgedNeoplasm StagingNeutrophilsPrognosisAmino AcidsBiomarkers, TumorCytokines

Identifiers

PMID30563990
PMCPMC6342921
OpenAlexW2903584355

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.