Evidence map›Paper›PMID 27905065›Full record

ArticleBulletin of mathematical biology2017

Spatial Measures of Genetic Heterogeneity During Carcinogenesis.

K Storey, M D Ryser, K Leder, J Foo

Abstract read
In one paragraph

Article in Bulletin of mathematical biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

4 authors.

K StoreyUniversity of Minnesota Twin Cities, Minneapolis, MN, USA.
M D RyserDepartment of Surgery, Division of Oncologic and GI Surgery, Duke University Medical Center, Durham, NC, USA.
K LederUniversity of Minnesota Twin Cities, Minneapolis, MN, USA.
J FooUniversity of Minnesota Twin Cities, Minneapolis, MN, USA. jyfoo@umn.edu.

Funding

Mathematical Models of Cancer Initiation, Progression, and Resistance to TherapyR01GM096190 · NIGMS · DUKE UNIVERSITY · PI DURRETT, RICK · 2010 to 2013
$1.4M
NIGMS NIH HHS R01 GM096190
6 · The paper itself

Abstract

In this work we explore the temporal dynamics of spatial heterogeneity during the process of tumorigenesis from healthy tissue. We utilize a spatial stochastic model of mutation accumulation and clonal expansion in a structured tissue to describe this process. Under a two-step tumorigenesis model, we first derive estimates of a non-spatial measure of diversity: Simpson's Index, which is the probability that two individuals sampled at random from the population are identical, in the premalignant population. We next analyze two new measures of spatial population heterogeneity. In particular we study the typical length scale of genetic heterogeneity during the carcinogenesis process and estimate the extent of a surrounding premalignant clone given a clinical observation of a premalignant point biopsy. This evolutionary framework contributes to a growing literature focused on developing a better understanding of the spatial population dynamics of cancer initiation and progression.

Indexed as

CarcinogenesisCocarcinogenesisComputer SimulationHumansMathematical ConceptsModels, GeneticMonte Carlo MethodMutationPrecancerous ConditionsStochastic ProcessesCarcinogenesisGenetic heterogeneitySpatial evolution

Identifiers

PMID27905065
PMCPMC6065111

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.