Evidence map›Paper›PMID 28943951›Full record

ArticleOncology letters2017

Recurrent alterations of the WW domain containing oxidoreductase gene spanning the common fragile site FRA16D in multiple myeloma and monoclonal gammopathy of undetermined significance.

Hiroshi Handa, Yoshiko Sasaki, Hikaru Hattori, Lobna Alkebsi, Tetsuhiro Kasamatsu, Takayuki Saitoh, Takeki Mitsui, Akihiko Yokohama, Norifumi Tsukamoto, Morio Matsumoto and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 17% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. B-cell-specificBlood neoplasia · 2025
    Article
  2. Frontiers in oncology · 2019
    Article
  3. Review
  4. Article
  5. Modeling WWOX Loss of FunctionFrontiers in oncology · 2018
    Review
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 3 institutions in 1 country.

Hiroshi HandaDepartment of Medicine and Clinical Science, Gunma University Graduate School of Medicine, Maebashi, Gunma 371-8511, Japan.
Yoshiko SasakiDepartment of Laboratory Science, Gunma University Graduate School of Medicine, Maebashi, Gunma 371-8511, Japan.
Hikaru HattoriDepartment of Laboratory Science, Gunma University Graduate School of Medicine, Maebashi, Gunma 371-8511, Japan.
Lobna AlkebsiDepartment of Laboratory Science, Gunma University Graduate School of Medicine, Maebashi, Gunma 371-8511, Japan.
Tetsuhiro KasamatsuDepartment of Laboratory Science, Gunma University Graduate School of Medicine, Maebashi, Gunma 371-8511, Japan.
Takayuki SaitohDepartment of Laboratory Science, Gunma University Graduate School of Medicine, Maebashi, Gunma 371-8511, Japan.
Takeki MitsuiDepartment of Medicine and Clinical Science, Gunma University Graduate School of Medicine, Maebashi, Gunma 371-8511, Japan.
Akihiko YokohamaBlood Transfusion Service, Gunma University Hospital, Maebashi, Gunma 371-8511, Japan.
Norifumi TsukamotoOncology Center, Gunma University Hospital, Maebashi, Gunma 371-8511, Japan.
Morio MatsumotoDepartment of Hematology, National Hospital Organization Shibukawa Medical Center, Shibukawa, Gunma 377-0280, Japan.
Hirokazu MurakamiDepartment of Laboratory Science, Gunma University Graduate School of Medicine, Maebashi, Gunma 371-8511, Japan.
Gunma University · JPGunma University Hospital · JPNational Hospital Organization · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The putative tumor suppressor gene WW domain containing oxidoreductase (WWOX) spans a common fragile site (CFS) on chromosome 16q23.3. CFSs are regions of profound genomic instability and sites for genomic deletions in cancer cells. Therefore, WWOX is structurally altered in diverse nonhematological cancer types. However, the function of WWOX in hematological tumor types, including multiple myeloma (MM) and monoclonal gammopathy of undetermined significance (MGUS) remains unclear. WWOX expression and methylation in patients with MM, MGUS, or noninvasive lymphoma (control) were analyzed using reverse transcription- and methylation specific-polymerase chain reaction analysis. Variant WWOX transcripts were detected in 65 and 50% of patients with MM and MGUS, respectively, compared with 10% of controls. WWOX expression was higher in patients with MM, and WWOX promoter methylation was detected in 35% of patients with MM compared with 5% of patients with MGUS and 4% of controls. WWOX promoter methylation was significantly associated with shorter overall survival time of patients, in particular those with MM who were never treated with novel agents. Genomic alterations, including deletions and promoter methylation that affect WWOX expression occur early and may be involved in the pathogenesis, progression, and prognosis of MM.

Indexed as

common fragile sitemethylationmonoclonal gammopathy of undetermined significancemultiple myelomaWW domain containing oxidoreductase gene

Identifiers

PMID28943951
PMCPMC5605961
OpenAlexW2737128405

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.