Evidence map›Paper›PMID 26465159›Full record

ArticlePloS one2015

Invariant Characteristics of Carcinogenesis.

Simon Sherman, Nirosha Rathnayake, Tengiz Mdzinarishvili

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 90% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

3 authors at 2 institutions in 2 countries.

Simon ShermanEppley Institute for Research in Cancer, University of Nebraska Medical Center, Omaha, Nebraska, United States of America; College of Public Health, University of Nebraska Medical Center, Omaha, Nebraska, United States of America.
Nirosha RathnayakeEppley Institute for Research in Cancer, University of Nebraska Medical Center, Omaha, Nebraska, United States of America; College of Public Health, University of Nebraska Medical Center, Omaha, Nebraska, United States of America.
Tengiz MdzinarishviliSchool of Natural Sciences and Engineering, Ilia State University, Tbilisi, Georgia.
University of Nebraska Medical Center · USIlia State University · GE

Funding

Enhancing the Biomedical Computing Platform for Pancreatic Cancer ResearchR01CA140940 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI SHERMAN, SIMON · 2010 to 2014
$1.5M
NCI NIH HHS 1 R01 CA140940-05NCI NIH HHS R01 CA140940
6 · The paper itself

Abstract

Carcinogenic modeling is aimed at mathematical descriptions of cancer development in aging. In this work, we assumed that a small fraction of individuals in the population is susceptible to cancer, while the rest of the population is resistant to cancer. For individuals susceptible to cancer we adopted methods of conditional survival analyses. We performed computational experiments using data on pancreatic, stomach, gallbladder, colon and rectum, liver, and esophagus cancers from the gastrointestinal system collected for men and women in the SEER registries during 1975-2009. In these experiments, we estimated the time period effects, the birth cohort effects, the age effects and the population (unconditional) cancer hazard rates. We also estimated the individual cancer presentation rates and the individual cancer resistance rates, which are, correspondingly, the hazard and survival rates conditioned on the susceptibility to cancer. The performed experiments showed that for men and women, patterns of the age effects, the individual cancer presentation rates and the individual cancer resistance rates are: (i) intrinsic for each cancer subtype, (ii) invariant to the place of living of the individuals diagnosed with cancer, and (iii) well adjusted for the modifiable variables averaged at a given time period. Such specificity and invariability of the age effects, the individual cancer presentation rates and the individual cancer resistance rates suggest that these carcinogenic characteristics can be useful for predictive carcinogenic studies by methods of inferential statistics and for the development of novel strategies for cancer prevention.

Indexed as

CarcinogenesisAdultAgedAged, 80 and overAge FactorsComputer SimulationFemaleGastrointestinal NeoplasmsHumansMaleMiddle AgedSEER Program

Identifiers

PMID26465159
PMCPMC4605720
OpenAlexW2218458879

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.