Evidence map›Paper›PMID 26339434›Full record

ArticleInternational journal of clinical and experimental pathology2015

Undifferentiated pleomorphic sarcoma with co-existence of KRAS/PIK3CA mutations.

Bingcheng Li, Li Li, Xiaoying Li, Yuanyuan Wang, Yuwen Xie, Chunxia Liu, Feng Li

Abstract readCase Reports
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Defining an embryonal rhabdomyosarcoma endotype.Cold Spring Harbor molecular case studies · 2020
    Article
  7. Article
  8. 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

7 authors.

Bingcheng LiDepartment of Pathology, Shihezi University School of Medicine and The Key Laboratories for Xinjiang Endemic and Ethnic Diseases, Chinese Ministry of Education Shihezi 832002, Xinjiang, China.
Li LiDepartment of Pathology, The First Affiliated Hospital, Shihezi University School of Medicine Shihezi 832002, Xinjiang, China.
Xiaoying LiDepartment of Pathology, Shihezi University School of Medicine and The Key Laboratories for Xinjiang Endemic and Ethnic Diseases, Chinese Ministry of Education Shihezi 832002, Xinjiang, China.
Yuanyuan WangDepartment of Pathology, Shihezi University School of Medicine and The Key Laboratories for Xinjiang Endemic and Ethnic Diseases, Chinese Ministry of Education Shihezi 832002, Xinjiang, China.
Yuwen XieDepartment of Pathology, Shihezi University School of Medicine and The Key Laboratories for Xinjiang Endemic and Ethnic Diseases, Chinese Ministry of Education Shihezi 832002, Xinjiang, China.
Chunxia LiuDepartment of Pathology, Shihezi University School of Medicine and The Key Laboratories for Xinjiang Endemic and Ethnic Diseases, Chinese Ministry of Education Shihezi 832002, Xinjiang, China ; Department of Pathology, The First Affiliated Hospital, Shihezi University School of Medicine Shihezi 832002, Xinjiang, China.
Feng LiDepartment of Pathology, Shihezi University School of Medicine and The Key Laboratories for Xinjiang Endemic and Ethnic Diseases, Chinese Ministry of Education Shihezi 832002, Xinjiang, China ; Department of Pathology, The First Affiliated Hospital, Shihezi University School of Medicine Shihezi 832002, Xinjiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundUndifferentiated pleomorphic sarcoma (UPS), previously known as malignant fibrous histiocytoma, comprises a series of high-grade soft tissue sarcomas, which fail to exhibit any specific line of differentiation by using currently available ancillary techniques. Studies on gene mutation screening occurring in UPS are rarely conducted. In this study, we described a case of UPS and analyzed its mutation changes. We detected 19 hotspot oncogenes in the case. To the best of our knowledge, this study is the first to use a high-throughput OncoCarta panel 1.0 and MassARRAY system to detect 238 known mutations in 19 hotspot oncogenes in UPS. In this study, our result revealed two missense mutations, namely, KRAS mutation (35G > A, G12D) and PIK3CA mutation (1636C > A, Q546K) in the case.

Indexed as

Cell DifferentiationMutation, MissenseAgedBiomarkers, TumorBiopsyClass I Phosphatidylinositol 3-KinasesDNA Mutational AnalysisFemaleGenetic Predisposition to DiseaseHigh-Throughput Nucleotide SequencingHistiocytoma, Malignant FibrousHumansImmunohistochemistryPhenotypePhosphatidylinositol 3-KinasesProto-Oncogene Proteins p21(ras)Biomarkers, TumorClass I Phosphatidylinositol 3-KinasesKRAS protein, humanPhosphatidylinositol 3-KinasesPIK3CA protein, humanProto-Oncogene Proteins p21(ras)MassARRAYmutationsUndifferentiated soft tissue sarcoma

Identifiers

PMID26339434
PMCPMC4555762

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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.