Evidence map›Paper›PMID 33919272›Full record

ReviewInternational journal of molecular sciences2021

Profiling Colorectal Cancer in the Landscape Personalized Testing-Advantages of Liquid Biopsy.

Donatella Verbanac, Andrea Čeri, Iva Hlapčić, Mehdi Shakibaei, Aranka Brockmueller, Božo Krušlin, Neven Ljubičić, Neven Baršić, Dijana Detel, Lara Batičić and 12 more

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–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

7 citing papers in PubMed.

  1. Article
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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

22 authors.

Donatella VerbanacDepartment of Medical Biochemistry and Hematology, Faculty of Pharmacy and Biochemistry, University of Zagreb, Ante Kovačića 1, 10000 Zagreb, Croatia.ORCID 0000-0002-9106-1604
Andrea ČeriDepartment of Medical Biochemistry and Hematology, Faculty of Pharmacy and Biochemistry, University of Zagreb, Ante Kovačića 1, 10000 Zagreb, Croatia.ORCID 0000-0003-3709-6328
Iva HlapčićDepartment of Medical Biochemistry and Hematology, Faculty of Pharmacy and Biochemistry, University of Zagreb, Ante Kovačića 1, 10000 Zagreb, Croatia.
Mehdi ShakibaeiMusculoskeletal Research Group and Tumour Biology, Faculty of Medicine, Institute of Anatomy, Ludwig-Maximilian-University Munich, Pettenkoferstrasse 11, D-80336 Munich, Germany.ORCID 0000-0002-6304-7506
Aranka BrockmuellerMusculoskeletal Research Group and Tumour Biology, Faculty of Medicine, Institute of Anatomy, Ludwig-Maximilian-University Munich, Pettenkoferstrasse 11, D-80336 Munich, Germany.
Božo KrušlinSchool of Medicine, University of Zagreb, Šalata 3, 10000 Zagreb, Croatia.
Neven LjubičićSchool of Medicine, University of Zagreb, Šalata 3, 10000 Zagreb, Croatia.ORCID 0000-0002-5207-4357
Neven BaršićSchool of Medicine, University of Zagreb, Šalata 3, 10000 Zagreb, Croatia.
Dijana DetelDepartment of Medical Chemistry, Biochemistry and Clinical Chemistry, Faculty of Medicine, Braće Branchetta 20/1, 51000 Rijeka, Croatia.
Lara BatičićDepartment of Medical Chemistry, Biochemistry and Clinical Chemistry, Faculty of Medicine, Braće Branchetta 20/1, 51000 Rijeka, Croatia.ORCID 0000-0002-2837-4157
Lada RumoraDepartment of Medical Biochemistry and Hematology, Faculty of Pharmacy and Biochemistry, University of Zagreb, Ante Kovačića 1, 10000 Zagreb, Croatia.
Anita Somborac-BačuraDepartment of Medical Biochemistry and Hematology, Faculty of Pharmacy and Biochemistry, University of Zagreb, Ante Kovačića 1, 10000 Zagreb, Croatia.ORCID 0000-0002-8573-4294
Mario ŠtefanovićDepartment of Medical Biochemistry and Hematology, Faculty of Pharmacy and Biochemistry, University of Zagreb, Ante Kovačića 1, 10000 Zagreb, Croatia.ORCID 0000-0002-3965-3231
Ivana ĆelapDepartment of Clinical Chemistry, University Hospital Centre "Sestre milosrdnice", University of Zagreb, Vinogradska 29, 10000 Zagreb, Croatia.ORCID 0000-0002-3982-5777
Alma DemirovićDepartment of Pathology and Cytology "Ljudevit Jurak", University Hospital Centre "Sestre milosrdnice", University of Zagreb, Vinogradska 29, 10000 Zagreb, Croatia.
Roberta PetlevskiDepartment of Medical Biochemistry and Hematology, Faculty of Pharmacy and Biochemistry, University of Zagreb, Ante Kovačića 1, 10000 Zagreb, Croatia.
József PetrikDepartment of Medical Biochemistry and Hematology, Faculty of Pharmacy and Biochemistry, University of Zagreb, Ante Kovačića 1, 10000 Zagreb, Croatia.
Marija Grdić RajkovićDepartment of Medical Biochemistry and Hematology, Faculty of Pharmacy and Biochemistry, University of Zagreb, Ante Kovačića 1, 10000 Zagreb, Croatia.
Andrea Hulina-TomaškovićDepartment of Medical Biochemistry and Hematology, Faculty of Pharmacy and Biochemistry, University of Zagreb, Ante Kovačića 1, 10000 Zagreb, Croatia.
Ivana RakoDepartment of Laboratory Diagnostics, University Hospital Centre Zagreb, University of Zagreb, Kišpatićeva 12, 10000 Zagreb, Croatia.ORCID 0000-0002-3292-9661
Luciano SasoDepartment of Physiology and Pharmacology "Vittorio Erspamer", Sapienza University of Rome, Piazzale Aldo Moro 5, 00185 Roma, Italy.ORCID 0000-0003-4530-8706
Karmela BarišićDepartment of Medical Biochemistry and Hematology, Faculty of Pharmacy and Biochemistry, University of Zagreb, Ante Kovačića 1, 10000 Zagreb, Croatia.

Funding

Hrvatska Zaklada za Znanost HRZZ IP-2019-04-4624
6 · The paper itself

Abstract

Drug-specific therapeutic approaches for colorectal cancer (CRC) have contributed to significant improvements in patient health. Nevertheless, there is still a great need to improve the personalization of treatments based on genetic and epigenetic tumor profiles to maximize the quality and efficacy while limiting cytotoxicity. Currently, CEA and CA 19-9 are the only validated blood biomarkers in clinical practice. For this reason, laboratories are trying to identify new specific prognostics and, more importantly, predictive biomarkers for CRC patient profiling. Thus, the unique landscape of personalized biomarker data should have a clinical impact on CRC treatment strategies and molecular genetic screening tests should become the standard method for diagnosing CRC. This review concentrates on recent molecular testing in CRC and discusses the potential modifications in CRC assay methodology with the upcoming clinical application of novel genomic approaches. While mechanisms for analyzing circulating tumor DNA have been proven too inaccurate, detecting and analyzing circulating tumor cells and protein analysis of exosomes represent more promising options. Blood liquid biopsy offers good prospects for the future if the results align with pathologists' tissue analyses. Overall, early detection, accurate diagnosis and treatment monitoring for CRC with specific markers and targeted molecular testing may benefit many patients.

Indexed as

Biomarkers, TumorCirculating Tumor DNAColorectal NeoplasmsHumansLiquid BiopsyMass ScreeningBiomarkers, TumorCirculating Tumor DNAbiomarkerscolorectal cancerCTCctDNAearly detection examinationexosomesliquid biopsypersonalized medicinetumor treatment

Identifiers

PMID33919272
PMCPMC8122648

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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.