Evidence map›Paper›PMID 32155840›Full record

ArticleInternational journal of molecular sciences2020

Similarities in the General Chemical Composition of Colon Cancer Cells and Their Microvesicles Investigated by Spectroscopic Methods-Potential Clinical Relevance.

Joanna Depciuch, Bartosz Klębowski, Małgorzata Stec, Rafał Szatanek, Kazimierz Węglarczyk, Monika Baj-Krzyworzeka, Magdalena Parlińska-Wojtan, Jarek Baran

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. 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
0.5field-weighted citation impact, top 38% 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

7 citing papers in PubMed, 14 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Joanna DepciuchInstitute of Nuclear Physics Polish Academy of Sciences, PL-31-342 Krakow, Poland.ORCID 0000-0003-0168-1701
Bartosz KlębowskiInstitute of Nuclear Physics Polish Academy of Sciences, PL-31-342 Krakow, Poland.ORCID 0000-0001-7962-1894
Małgorzata StecDepartment of Clinical Immunology, Institute of Pediatrics, Jagiellonian University Medical College, PL-30-663 Krakow, Poland.
Rafał SzatanekDepartment of Clinical Immunology, Institute of Pediatrics, Jagiellonian University Medical College, PL-30-663 Krakow, Poland.
Kazimierz WęglarczykDepartment of Clinical Immunology, Institute of Pediatrics, Jagiellonian University Medical College, PL-30-663 Krakow, Poland.
Monika Baj-KrzyworzekaDepartment of Clinical Immunology, Institute of Pediatrics, Jagiellonian University Medical College, PL-30-663 Krakow, Poland.
Magdalena Parlińska-WojtanInstitute of Nuclear Physics Polish Academy of Sciences, PL-31-342 Krakow, Poland.ORCID 0000-0001-5901-400X
Jarek BaranDepartment of Clinical Immunology, Institute of Pediatrics, Jagiellonian University Medical College, PL-30-663 Krakow, Poland.ORCID 0000-0003-1787-1972
Jagiellonian University · PLInstitute of Nuclear Physics, Polish Academy of Sciences · PL

Funding

European Commission H2020-MSCA-RISE-2017 "CANCER" No. 777682European Commission "POWER" POWR.03.02.00-00-I013/16
6 · The paper itself

Abstract

Colon cancer constitutes 33% of all cancer cases in humans and the majority of patients with metastatic colon cancer still have poor prognosis. An important role in cancer development is the communication between cancer and normal cells. This may occur, among others, through extracellular vesicles (including microvesicles) (MVs), which are being released by both types of cells. MVs may regulate a diverse range of biological processes and are considered as useful cancer biomarkers. Herein, we show that similarity in the general chemical composition between colon cancer cells and their corresponding tumor-derived microvesicles (TMVs) does exist. These results have been confirmed by spectroscopic methods for four colon cancer cell lines: HCT116, LoVo, SW480, and SW620 differing in their aggressiveness/metastatic potential. Our results show that Raman and Fourier Transform InfraRed (FTIR) analysis of the cell lines and their corresponding TMVs did not differ significantly in the characterization of their chemical composition. However, hierarchical cluster analysis of the data obtained by both of the methods revealed that only Raman spectroscopy provides results that are in line with the molecular classification of colon cancer, thus having potential clinical relevance.

Indexed as

Biomarkers, TumorCell-Derived MicroparticlesColonic NeoplasmsHumansSpectroscopy, Fourier Transform InfraredSpectrum Analysis, RamanTumor Cells, CulturedBiomarkers, Tumorcolon cancerextracellular vesiclesFTIR spectroscopyFT-Raman spectroscopyHCT116 cellsLoVo cellsSW480 cellsSW620 cellstumor-derived microvesicles

Identifiers

PMID32155840
PMCPMC7084448
OpenAlexW3010388243

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.