Evidence map›Paper›PMID 35454948›Full record

ArticleCancers2022

Integrated Network Pharmacology Approach for Drug Combination Discovery: A Multi-Cancer Case Study.

Antonio Federico, Michele Fratello, Giovanni Scala, Lena Möbus, Alisa Pavel, Giusy Del Giudice, Michele Ceccarelli, Valerio Costa, Alfredo Ciccodicola, Vittorio Fortino and 2 more

Abstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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  5. Article
  6. Review
  7. Review
  8. PHGDH: a novel therapeutic target in cancer.Experimental & molecular medicine · 2024
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
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

12 authors.

Antonio FedericoFinnish Hub for Development and Validation of Integrated Approaches (FHAIVE), Tampere University, 33100 Tampere, Finland.ORCID 0000-0003-2554-9879
Michele FratelloFinnish Hub for Development and Validation of Integrated Approaches (FHAIVE), Tampere University, 33100 Tampere, Finland.ORCID 0000-0002-3997-2339
Giovanni ScalaDepartment of Biology, University of Naples "Federico II", 80138 Naples, Italy.
Lena MöbusFinnish Hub for Development and Validation of Integrated Approaches (FHAIVE), Tampere University, 33100 Tampere, Finland.
Alisa PavelFinnish Hub for Development and Validation of Integrated Approaches (FHAIVE), Tampere University, 33100 Tampere, Finland.
Giusy Del GiudiceFinnish Hub for Development and Validation of Integrated Approaches (FHAIVE), Tampere University, 33100 Tampere, Finland.ORCID 0000-0003-0999-4796
Michele CeccarelliDepartment of Electrical Engineering and Information Technology (DIETI), University of Naples "Federico II", 80138 Naples, Italy.
Valerio CostaInstitute of Genetics and Biophysics "Adriano Buzzati-Traverso", CNR, Via P. Castellino 111, 80131 Naples, Italy.ORCID 0000-0002-7294-6933
Alfredo CiccodicolaInstitute of Genetics and Biophysics "Adriano Buzzati-Traverso", CNR, Via P. Castellino 111, 80131 Naples, Italy.ORCID 0000-0002-9924-1482
Vittorio FortinoSchool of Medicine, Institute of Biomedicine, University of Eastern Finland, 70211 Kuopio, Finland.ORCID 0000-0001-8693-5285
Angela SerraFinnish Hub for Development and Validation of Integrated Approaches (FHAIVE), Tampere University, 33100 Tampere, Finland.ORCID 0000-0002-3374-1492
Dario GrecoFinnish Hub for Development and Validation of Integrated Approaches (FHAIVE), Tampere University, 33100 Tampere, Finland.ORCID 0000-0001-9195-9003

Funding

HPC-EUROPA3 INFRAIA-2016-1-730897
6 · The paper itself

Abstract

Despite remarkable efforts of computational and predictive pharmacology to improve therapeutic strategies for complex diseases, only in a few cases have the predictions been eventually employed in the clinics. One of the reasons behind this drawback is that current predictive approaches are based only on the integration of molecular perturbation of a certain disease with drug sensitivity signatures, neglecting intrinsic properties of the drugs. Here we integrate mechanistic and chemocentric approaches to drug repositioning by developing an innovative network pharmacology strategy. We developed a multilayer network-based computational framework integrating perturbational signatures of the disease as well as intrinsic characteristics of the drugs, such as their mechanism of action and chemical structure. We present five case studies carried out on public data from The Cancer Genome Atlas, including invasive breast cancer, colon adenocarcinoma, lung squamous cell carcinoma, hepatocellular carcinoma and prostate adenocarcinoma. Our results highlight paclitaxel as a suitable drug for combination therapy for many of the considered cancer types. In addition, several non-cancer-related genes representing unusual drug targets were identified as potential candidates for pharmacological treatment of cancer.

Indexed as

cancercancer therapydrug combinationsdruggabilitydrug repositioningnetworksystems pharmacology

Identifiers

PMID35454948
PMCPMC9028433

What OpenQuestion holds

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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.