Evidence map›Paper›PMID 29222441›Full record

ArticleNature communications2017

Robust RNA-based in situ mutation detection delineates colorectal cancer subclonal evolution.

Ann-Marie Baker, Weini Huang, Xiao-Ming Mindy Wang, Marnix Jansen, Xiao-Jun Ma, Jeffrey Kim, Courtney M Anderson, Xingyong Wu, Liuliu Pan, Nan Su and 11 more

Open access · goldAbstract readMulticenter StudyValidation StudyVideo-Audio Media
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

42 citing papers in PubMed, 79 citations in OpenAlex.

  1. Article
  2. Use of Automated BaseScope Assay on the Leica BOND RX.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Spatial biology of cancer evolution.Nature reviews. Genetics · 2023
    Review
  10. Article
  11. Article
  12. Predicting Molecular Subtype and Survival of Rhabdomyosarcoma Patients Using Deep Learning of H&E Images: A Report from the Children's Oncology Group.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Article
  13. Article
  14. Defining the spatial landscape of KRAS mutated congenital pulmonary airway malformations: a distinct entity with a spectrum of histopathologic features.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2022
    Article
  15. Article
  16. Article
  17. 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

21 authors at 7 institutions in 2 countries.

Ann-Marie BakerBarts Cancer Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, EC1M 6BQ, UK. a.m.c.baker@qmul.ac.uk.
Weini HuangBarts Cancer Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, EC1M 6BQ, UK.
Xiao-Ming Mindy WangAdvanced Cell Diagnostics, Newark, CA, 94560, USA.
Marnix JansenDepartment of Histopathology, University College London Hospital, London, WC1E 6JJ, UK.
Xiao-Jun MaAdvanced Cell Diagnostics, Newark, CA, 94560, USA.
Jeffrey KimAdvanced Cell Diagnostics, Newark, CA, 94560, USA.
Courtney M AndersonAdvanced Cell Diagnostics, Newark, CA, 94560, USA.
Xingyong WuAdvanced Cell Diagnostics, Newark, CA, 94560, USA.
Liuliu PanAdvanced Cell Diagnostics, Newark, CA, 94560, USA.
Nan SuAdvanced Cell Diagnostics, Newark, CA, 94560, USA.
Yuling LuoAdvanced Cell Diagnostics, Newark, CA, 94560, USA.
Enric DomingoDepartment of Oncology, Old Road Campus Research Building, University of Oxford, Roosevelt Drive, Oxford, OX3 7DQ, UK.
Timon HeideCentre for Evolution and Cancer, The Institute of Cancer Research, 15 Cotswold Road, Sutton, London, SM2 5NG, UK.
Andrea SottorivaCentre for Evolution and Cancer, The Institute of Cancer Research, 15 Cotswold Road, Sutton, London, SM2 5NG, UK.ORCID http://orcid.org/0000-0001-6709-9533
Annabelle LewisCancer Gene Regulation Laboratory, Centre for Cancer Gene Research, Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford, OX3 7BN, UK.
Andrew D BeggsSurgical Research Laboratory, Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, B15 2TT, UK.ORCID http://orcid.org/0000-0003-0784-2967
Nicholas A WrightBarts Cancer Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, EC1M 6BQ, UK.
Manuel Rodriguez-JustoDepartment of Histopathology, University College London Hospital, London, WC1E 6JJ, UK.
Emily ParkAdvanced Cell Diagnostics, Newark, CA, 94560, USA.
Ian TomlinsonCancer Genetics and Evolution Laboratory, Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, B15 2TT, UK. i.tomlinson@bham.ac.uk.ORCID http://orcid.org/0000-0003-3037-1470
Trevor A GrahamBarts Cancer Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, EC1M 6BQ, UK. t.graham@qmul.ac.uk.ORCID http://orcid.org/0000-0001-9582-1597
Advanced Cell Diagnostics (United States) · USQueen Mary University of London · GBInstitute of Cancer Research · GBUniversity College Hospital · GBUniversity of Birmingham · GBCentre for Human Genetics · GBUniversity of Oxford · GB

Funding

Cancer Research UK 105104/Z/14/ZCancer Research UK 14895Cancer Research UK 16459Cancer Research UK 19771Cancer Research UK 22745Cancer Research UK 22909Cancer Research UK A14895Cancer Research UK A19771Cancer Research UK A21870Cancer Research UK A22745Cancer Research UK A23923Cancer Research UK C52506/A22909Medical Research Council MR/M009157/1Medical Research Council MR/M016587/1Wellcome TrustWellcome Trust 090532/Z/09/ZWellcome Trust 102732/Z/13/ZWellcome Trust 202778/B/16/ZWellcome Trust 202778/Z/16/Z
6 · The paper itself

Abstract

Intra-tumor heterogeneity (ITH) is a major underlying cause of therapy resistance and disease recurrence, and is a read-out of tumor growth. Current genetic ITH analysis methods do not preserve spatial context and may not detect rare subclones. Here, we address these shortfalls by developing and validating BaseScope-a novel mutation-specific RNA in situ hybridization assay. We target common point mutations in the BRAF, KRAS and PIK3CA oncogenes in archival colorectal cancer samples to precisely map the spatial and morphological context of mutant subclones. Computational modeling suggests that subclones must arise sufficiently early, or carry a considerable fitness advantage, to form large or spatially disparate subclones. Examples of putative treatment-resistant cells isolated in small topographical areas are observed. The BaseScope assay represents a significant technical advance for in situ mutation detection that provides new insight into tumor evolution, and could have ramifications for selecting patients for treatment.

Indexed as

Cell Line, TumorClass I Phosphatidylinositol 3-KinasesClonal EvolutionColorectal NeoplasmsComputer SimulationDNA Mutational AnalysisDrug Resistance, NeoplasmHumansIn Situ HybridizationNeoplasm Recurrence, LocalPoint MutationProto-Oncogene Proteins B-rafProto-Oncogene Proteins p21(ras)RNABRAF protein, humanClass I Phosphatidylinositol 3-KinasesKRAS protein, humanPIK3CA protein, humanProto-Oncogene Proteins B-rafProto-Oncogene Proteins p21(ras)RNA

Identifiers

PMID29222441
PMCPMC5722928
OpenAlexW2774431250

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.