Evidence map›Paper›PMID 30854179›Full record

ArticleJournal of public health in Africa2018

The potential of RNA as a target for national screening of pre-cancer.

Frank Karlsen, Margaret Muturi, Cosmas Muyabwa, Lars E Roseng, Serge Bigabwa, Byamungu Chihongola, Lucy Muchiri

Open access · goldAbstract read
In one paragraph

Article in Journal of public health in Africa, 2018. 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
0.2field-weighted citation impact, top 42% 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

7 authors at 1 institution in 1 country.

Frank KarlsenDepartment of Micro- and Nanosystem Technology, University College of Southeast Norway, Borre, Norway.
Margaret MuturiDepartment of Micro- and Nanosystem Technology, University College of Southeast Norway, Borre, Norway.
Cosmas MuyabwaDepartment of Micro- and Nanosystem Technology, University College of Southeast Norway, Borre, Norway.
Lars E RosengDepartment of Micro- and Nanosystem Technology, University College of Southeast Norway, Borre, Norway.
Serge BigabwaDepartment of Micro- and Nanosystem Technology, University College of Southeast Norway, Borre, Norway.
Byamungu ChihongolaDepartment of Micro- and Nanosystem Technology, University College of Southeast Norway, Borre, Norway.
Lucy MuchiriDepartment of Micro- and Nanosystem Technology, University College of Southeast Norway, Borre, Norway.
University of South-Eastern Norway · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Whole national screening of pre-cancer is done only in some few countries, dominated by The Netherlands, Denmark, UK, Norway and Finland. These national screenings are done combining national cancer registry, national public health and national medical bodies or hospitals. Until some few years ago national screening was only done using morphological or visual methods or technology. Today a number of molecular methods have been implemented to serve these national screening programs. Based on all the discussions within this review, it is clear that the main driving engine and the cause of cervical pre-cancer and the main cause of invasive cervical cancer is the expression of E6 and E7 oncoproteins from HPV 16, 18, 31, 33 and 45. However, the main challenge is the role of morphology or imaging-based diagnosis in the original definition of pre-cancer disease. This definition is not based on the cause of cervical precancer but based on a complex, subjective, morphological observations. The difference between these two definitions are discussed in this review. The unique discovery done while validating the first standardized detection technology used against mRNA, confirmed that the presence of both abnormal E6 and/or E7 mRNA and protein is the cause of cervical pre-cancer or severe neoplasia and the main cause of invasive cervical cancer. This confirmation was evident even though all these studies were disturbed by the above defined biases from morphology or imaging-based diagnosis. The use of the screening target that cause stable and high expression of the most carcinogenic compounds ever discovered, must cause a more accurate screening program. A number of studies have proved that the detection of E6/E7 mRNA followed-up by indirect or direct treatment in a well-organized national screening program, would reduce the incidence of cervical cancer. This review discusses the main studies involved in the scientific, clinical evaluation and how this unique technology could be used as a new medical gold standard for national screening of cervical pre-cancer.

Indexed as

oncologyPreventive healthcarepublic healthscreening in Africascreening of cervical pre-cancer

Identifiers

PMID30854179
PMCPMC6379696
OpenAlexW2906458891

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.