Evidence map›Paper›PMID 35343095›Full record

ArticleCancer medicine2022

Exploration of predictive biomarkers for postoperative recurrence of stage II/III colorectal cancer using genomic sequencing.

Fumishi Kishigami, Yosuke Tanaka, Yoko Yamamoto, Toshihide Ueno, Shinya Kojima, Kazuhito Sato, Satoshi Inoue, Saori Sugaya, Soichiro Ishihara, Hiroyuki Mano and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 48% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
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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

11 authors at 1 institution in 1 country.

Fumishi KishigamiDivision of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.
Yosuke TanakaDivision of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.
Yoko YamamotoDepartment of Surgical Oncology, The University of Tokyo, Tokyo, Japan.
Toshihide UenoDivision of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.
Shinya KojimaDivision of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.
Kazuhito SatoDepartment of Surgical Oncology, The University of Tokyo, Tokyo, Japan.
Satoshi InoueDivision of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.
Saori SugayaDivision of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.
Soichiro IshiharaDepartment of Surgical Oncology, The University of Tokyo, Tokyo, Japan.
Hiroyuki ManoDivision of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.ORCID 0000-0003-4645-0181
Masahito KawazuDivision of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.ORCID 0000-0003-4146-3629
The University of Tokyo · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Postoperative recurrence of colorectal cancer (CRC) eventually leads to therapeutic failure; therefore, treatment strategies based on accurate prediction of recurrence are urgently required. To identify biomarkers that can predict treatment outcomes, we compared the mutational profiles of surgically resected specimens from patients with recurrent cancer with those from patients with non-recurrent cancer. Target sequencing, whole-exome sequencing (WES), or whole-genome sequencing (WGS) was performed on 89 and 58 tumors from recurrent and non-recurrent cases, respectively. WGS revealed the driver mutations that were not detected with target sequencing or WES, including the structural variations affecting ZFP36L2. Loss of function of ZFP36L2 was frequently observed in primary tumors from recurrent cases. Furthermore, the recurrence-free survival of patients with loss of function of ZFP36L2 was significantly shorter relative to patients with no loss of ZFP36L2 function. In summary, the study demonstrated that detailed genomic analysis could help improve precision medicine for CRC.

Indexed as

Colorectal NeoplasmsNeoplasm Recurrence, LocalBiomarkersBiomarkers, TumorExome SequencingGenomicsHumansMutationBiomarkersBiomarkers, Tumorcolorectal cancerprecision medicinewhole genome sequenceZFP36L2

Identifiers

PMID35343095
PMCPMC9487878
OpenAlexW4220794761

What OpenQuestion holds

Textmetadata
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.