Evidence map›Paper›PMID 34795259›Full record

SynthesisNature communications2021

Modulation of pancreatic cancer cell sensitivity to FOLFIRINOX through microRNA-mediated regulation of DNA damage.

Pietro Carotenuto, Francesco Amato, Andrea Lampis, Colin Rae, Somaieh Hedayat, Maria C Previdi, Domenico Zito, Maya Raj, Vincenza Guzzardo, Francesco Sclafani and 28 more

Open access · goldAbstract readSystematic Review
In one paragraph

Synthesis in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.9field-weighted citation impact, top 7% 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

25 citing papers in PubMed, 45 citations in OpenAlex.

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  16. miRNAs in pancreatic cancer progression and metastasis.Clinical & experimental metastasis · 2024
    Review
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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

38 authors at 6 institutions in 3 countries.

Pietro Carotenuto *Division of Cancer Therapeutics, The Institute of Cancer Research, London, UK.ORCID http://orcid.org/0000-0002-6622-183X
Francesco Amato *Institute of Cancer Sciences, University of Glasgow, Glasgow, UK.
Andrea Lampis *Division of Molecular Pathology, The Institute of Cancer Research, London, UK.
Colin RaeInstitute of Cancer Sciences, University of Glasgow, Glasgow, UK.ORCID http://orcid.org/0000-0003-4432-6670
Somaieh HedayatDivision of Molecular Pathology, The Institute of Cancer Research, London, UK.
Maria C PrevidiDivision of Cancer Therapeutics, The Institute of Cancer Research, London, UK.
Domenico ZitoDivision of Molecular Pathology, The Institute of Cancer Research, London, UK.
Maya RajDivision of Cancer Therapeutics, The Institute of Cancer Research, London, UK.
Vincenza GuzzardoDepartment of Medicine, University of Padua, Padua, Italy.
Francesco SclafaniThe Royal Marsden NHS Trust, London and Surrey, London, UK.
Andrea LaneseThe Royal Marsden NHS Trust, London and Surrey, London, UK.
Claudia ParisiThe Royal Marsden NHS Trust, London and Surrey, London, UK.
Caterina VicentiniARC-Net Research Centre and Department of Diagnostics and Public Health, Section of Pathology, , University of Verona, Verona, Italy.
Ian Said-HuntingfordDivision of Cancer Therapeutics, The Institute of Cancer Research, London, UK.
Jens C HahneDivision of Molecular Pathology, The Institute of Cancer Research, London, UK.
Albert HallsworthDivision of Cancer Therapeutics, The Institute of Cancer Research, London, UK.
Vladimir KirkinDivision of Cancer Therapeutics, The Institute of Cancer Research, London, UK.
Kate YoungThe Royal Marsden NHS Trust, London and Surrey, London, UK.
Ruwaida BegumThe Royal Marsden NHS Trust, London and Surrey, London, UK.
Andrew WotherspoonThe Royal Marsden NHS Trust, London and Surrey, London, UK.
Kyriakos KouvelakisThe Royal Marsden NHS Trust, London and Surrey, London, UK.
Sergio Xavier AzevedoThe Royal Marsden NHS Trust, London and Surrey, London, UK.
Vasiliki MichalareaThe Royal Marsden NHS Trust, London and Surrey, London, UK.
Rosie Upstill-GoddardInstitute of Cancer Sciences, University of Glasgow, Glasgow, UK.ORCID http://orcid.org/0000-0002-2666-0934
Sheela RaoThe Royal Marsden NHS Trust, London and Surrey, London, UK.
David WatkinsThe Royal Marsden NHS Trust, London and Surrey, London, UK.
Naureen StarlingThe Royal Marsden NHS Trust, London and Surrey, London, UK.
Anguraj SadanandamDivision of Molecular Pathology, The Institute of Cancer Research, London, UK.ORCID http://orcid.org/0000-0001-8485-5150
David K ChangInstitute of Cancer Sciences, University of Glasgow, Glasgow, UK.ORCID http://orcid.org/0000-0002-4821-3078
Andrew V BiankinInstitute of Cancer Sciences, University of Glasgow, Glasgow, UK.ORCID http://orcid.org/0000-0002-0362-5597
Nigel B JamiesonInstitute of Cancer Sciences, University of Glasgow, Glasgow, UK.ORCID http://orcid.org/0000-0002-9552-4725
Aldo ScarpaARC-Net Research Centre and Department of Diagnostics and Public Health, Section of Pathology, , University of Verona, Verona, Italy.ORCID http://orcid.org/0000-0003-1678-739X
David CunninghamThe Royal Marsden NHS Trust, London and Surrey, London, UK.ORCID http://orcid.org/0000-0001-5158-1069
Ian ChauThe Royal Marsden NHS Trust, London and Surrey, London, UK.ORCID http://orcid.org/0000-0003-0286-8703
Paul WorkmanDivision of Cancer Therapeutics, The Institute of Cancer Research, London, UK.ORCID http://orcid.org/0000-0003-1659-3034
Matteo FassanDepartment of Medicine, University of Padua, Padua, Italy.ORCID http://orcid.org/0000-0001-6515-5482
Nicola ValeriDivision of Molecular Pathology, The Institute of Cancer Research, London, UK.ORCID http://orcid.org/0000-0002-5426-5683
Chiara BraconiDivision of Cancer Therapeutics, The Institute of Cancer Research, London, UK. chiara.braconi@glasgow.ac.uk.ORCID http://orcid.org/0000-0003-4835-1259
Royal Marsden NHS Foundation Trust · GBInstitute of Cancer Research · GBGlasgow Royal Infirmary · GBUniversity of Glasgow · GBUniversity of Padua · ITUniversity of Verona · IT

Funding

Cancer Research UK 18052Cancer Research UK C55370/A25813Wellcome Trust
6 · The paper itself

Abstract

FOLFIRINOX, a combination of chemotherapy drugs (Fluorouracil, Oxaliplatin, Irinotecan -FOI), provides the best clinical benefit in pancreatic ductal adenocarcinoma (PDAC) patients. In this study we explore the role of miRNAs (MIR) as modulators of chemosensitivity to identify potential biomarkers of response. We find that 41 and 84 microRNA inhibitors enhance the sensitivity of Capan1 and MiaPaCa2 PDAC cells respectively. These include a MIR1307-inhibitor that we validate in further PDAC cell lines. Chemotherapy-induced apoptosis and DNA damage accumulation are higher in MIR1307 knock-out (MIR1307KO) versus control PDAC cells, while re-expression of MIR1307 in MIR1307KO cells rescues these effects. We identify binding of MIR1307 to CLIC5 mRNA through covalent ligation of endogenous Argonaute-bound RNAs cross-linking immunoprecipitation assay. We validate these findings in an in vivo model with MIR1307 disruption. In a pilot cohort of PDAC patients undergoing FOLFIRONX chemotherapy, circulating MIR1307 correlates with clinical outcome.

Indexed as

DNA DamageGene Expression Regulation, NeoplasticAntineoplastic Combined Chemotherapy ProtocolsCarcinoma, Pancreatic DuctalFluorouracilHumansIrinotecanKaplan-Meier EstimateLeucovorinMicroRNAsNeoadjuvant TherapyOutcome Assessment, Health CareOxaliplatinPancreatic NeoplasmsFluorouracilIrinotecanLeucovorinMicroRNAsMIRN1307 microRNA, humanOxaliplatin

Identifiers

PMID34795259
PMCPMC8602334
OpenAlexW3213003275

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.