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pmid:31213644

Locally advanced rectal cancer transcriptomic-based secretome analysis reveals novel biomarkers useful to identify patients according to neoadjuvant chemoradiotherapy response.

Luisa Matos do Canto · Sarah Santiloni Cury · Mateus Camargo Barros-Filho · Bruna Elisa Catin Kupper · Maria Dirlei Ferreira de Souza Begnami · Cristovam Scapulatempo-Neto · Robson Francisco Carvalho · Fabio Albuquerque Marchi · Dorte Aalund Olsen · Jonna Skov Madsen · Birgitte Mayland Havelund · Samuel Aguiar · Silvia Regina Rogatto

Scientific reports · 2019 doi:10.1038/s41598-019-45151-w

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Experiment

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Data

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title
Locally advanced rectal cancer transcriptomic-based secretome analysis reveals novel biomarkers useful to identify patients according to neoadjuvant chemoradiotherapy response.
doi
10.1038/s41598-019-45151-w
pmid
31213644
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[0]
Luisa Matos do Canto
[1]
Sarah Santiloni Cury
[2]
Mateus Camargo Barros-Filho
[3]
Bruna Elisa Catin Kupper
[4]
Maria Dirlei Ferreira de Souza Begnami
[5]
Cristovam Scapulatempo-Neto
[6]
Robson Francisco Carvalho
[7]
Fabio Albuquerque Marchi
[8]
Dorte Aalund Olsen
[9]
Jonna Skov Madsen
[10]
Birgitte Mayland Havelund
[11]
Samuel Aguiar
[12]
Silvia Regina Rogatto
journal
Scientific reports
year
2019
abstract
Most patients with locally advanced rectal cancer (LARC) present incomplete pathological response (pIR) to neoadjuvant chemoradiotherapy (nCRT). Despite the efforts to predict treatment response using tumor-molecular features, as differentially expressed genes, no molecule has proved to be a strong biomarker. The tumor secretome analysis is a promising strategy for biomarkers identification, which can be assessed using transcriptomic data. We performed transcriptomic-based secretome analysis to select potentially secreted proteins using an in silico approach. The tumor expression profile of 28 LARC biopsies collected before nCRT was compared with normal rectal tissues (NT). The expression profile showed no significant differences between complete (pCR) and incomplete responders to nCRT. Genes with increased expression (pCR = 106 and pIR = 357) were used for secretome analysis based on public databases (Vesiclepedia, Human Cancer Secretome, and Plasma Proteome). Seventeen potentially secreted candidates (pCR = 1, pIR = 13 and 3 in both groups) were further investigated in two independent datasets (TCGA and GSE68204) confirming their over-expression in LARC and association with nCRT response (GSE68204). The expression of circulating amphiregulin and cMET proteins was confirmed in serum from 14 LARC patients. Future studies in liquid biopsies could confirm the utility of these proteins for personalized treatment in LARC patients.
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Locally advanced rectal cancer transcriptomic-based secretome analysis according to neoadjuvant chemoradiotherapy response
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Clinical and histopathological features of 42 locally advanced rectal cancer patients (28 evaluated by transcriptome analysis and 14 for protein expression in serum samples).
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Clinical and histopathological features of 42 locally advanced rectal cancer patients (28 evaluated by transcriptome analysis and 14 for protein expression in serum samples).
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Gene expression levels (FC: fold change) of the potentially secreted biomarkers in the discovery and validation set of rectal cancer compared with normal rectal tissues.
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In silico validation of potential biomarkers of nCRT response
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Gene expression levels (FC: fold change) of the potentially secreted biomarkers in the discovery and validation set of rectal cancer compared with normal rectal tissues.
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Quantification of and cMET and AREG protein in serum from 14 LARC patients.
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Serum values of amphiregulin and cMET from LARC patients
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Quantification of and cMET and AREG protein in serum from 14 LARC patients.
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Complete file
{"sci_version": "1.0", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:31213644", "kind": "science-record", "revision": 3, "content_hash": "sha256:394e06a22f4ebe1b44aa882317398390aee7880eb2ee2de09f061c4602caec6e", "created_at": "2026-11-01T15:40:46Z", "updated_at": "2026-11-01T18:50:56Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Locally advanced rectal cancer transcriptomic-based secretome analysis reveals novel biomarkers useful to identify patients according to neoadjuvant chemoradiotherapy response.", "doi": "10.1038/s41598-019-45151-w", "pmid": "31213644", "authors": ["Luisa Matos do Canto", "Sarah Santiloni Cury", "Mateus Camargo Barros-Filho", "Bruna Elisa Catin Kupper", "Maria Dirlei Ferreira de Souza Begnami", "Cristovam Scapulatempo-Neto", "Robson Francisco Carvalho", "Fabio Albuquerque Marchi", "Dorte Aalund Olsen", "Jonna Skov Madsen", "Birgitte Mayland Havelund", "Samuel Aguiar", "Silvia Regina Rogatto"], "journal": "Scientific reports", "year": 2019, "abstract": "Most patients with locally advanced rectal cancer (LARC) present incomplete pathological response (pIR) to neoadjuvant chemoradiotherapy (nCRT). Despite the efforts to predict treatment response using tumor-molecular features, as differentially expressed genes, no molecule has proved to be a strong biomarker. The tumor secretome analysis is a promising strategy for biomarkers identification, which can be assessed using transcriptomic data. We performed transcriptomic-based secretome analysis to select potentially secreted proteins using an in silico approach. The tumor expression profile of 28 LARC biopsies collected before nCRT was compared with normal rectal tissues (NT). The expression profile showed no significant differences between complete (pCR) and incomplete responders to nCRT. Genes with increased expression (pCR = 106 and pIR = 357) were used for secretome analysis based on public databases (Vesiclepedia, Human Cancer Secretome, and Plasma Proteome). Seventeen potentially secreted candidates (pCR = 1, pIR = 13 and 3 in both groups) were further investigated in two independent datasets (TCGA and GSE68204) confirming their over-expression in LARC and association with nCRT response (GSE68204). The expression of circulating amphiregulin and cMET proteins was confirmed in serum from 14 LARC patients. 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