Evidence map›Paper›PMID 33047659›Full record

ArticleTechnology in cancer research & treatment

Clinical-Pathologic Analysis of Breast Cancer With PIK3CA Mutations in Chinese Women.

Jing Lian, En-Wei Xu, Yan-Feng Xi, Hui-Wen Wang, Peng Bu, Jin-Fen Wang, Li-Xia Wang

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Article in Technology in cancer research & treatment. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 18% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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  8. Current oncology (Toronto, Ont.) · 2022
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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 at 2 institutions in 1 country.

Jing LianDepartment of Pathology, Shanxi Provincial Cancer Hospital, Taiyuan, Shanxi, People's Republic of China.ORCID 0000-0001-9753-1980
En-Wei XuDepartment of Pathology, Shanxi Provincial Cancer Hospital, Taiyuan, Shanxi, People's Republic of China.
Yan-Feng XiDepartment of Pathology, Shanxi Provincial Cancer Hospital, Taiyuan, Shanxi, People's Republic of China.
Hui-Wen WangDepartment of Pathology, Shanxi Provincial Cancer Hospital, Taiyuan, Shanxi, People's Republic of China.
Peng BuDepartment of Pathology, Shanxi Provincial Cancer Hospital, Taiyuan, Shanxi, People's Republic of China.
Jin-Fen WangDepartment of Pathology, Shanxi Provincial Cancer Hospital, Taiyuan, Shanxi, People's Republic of China.
Li-Xia WangDepartment of Pathology, Shanxi Provincial Cancer Hospital, Taiyuan, Shanxi, People's Republic of China.
Shanxi Provincial Cancer Hospital · CNShanxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeMutations of PIK3CA have recently been shown to play an important role in the pathogenesis and progression of breast neoplasms. The prevalence of PIK3CA in Chinese breast cancer patients may be underestimated. Therefore, we investigated the distribution of somatic PIK3CA mutation in Chinese breast cancer patients and explored their role in tumor phenotypes.

methodsMutational analysis of PIK3CA was done in 113 primary breast cancers of Chinese women used Amplification refractory mutation system (ARMS). The relationship of PIK3CA mutations with several clinicopathologic characteristics was analyzed.

resultsPIK3CA gene mutation was identified in 43(38.05%) cases and has a more significant difference between exon 9 and 20. HER2 gene amplification was 32.6% in 43 cases of PIK3CA mutation, but 37.1% in 70 cases of non-mutation (χ

conclusionA high frequency of somatic PIK3CA mutation was detected in Chinese breast cancer patients, especially in exon 20. The relationship between PIK3CA gene mutation and clinical pathological features of breast cancer needs to be further studied in a large series of patients. PIK3CA mutations seem to have the potential to be used in target treatment and as an indicator of prognosis.

Indexed as

MutationAdultAgedAged, 80 and overBreast NeoplasmsChinaClass I Phosphatidylinositol 3-KinasesDNA Mutational AnalysisFemaleGene AmplificationHumansImmunohistochemistryIn Situ Hybridization, FluorescenceMiddle AgedMutation RateNeoplasm GradingClass I Phosphatidylinositol 3-KinasesPIK3CA protein, humanARMSbreast cancerChineseclinicopathologic characteristicsPIK3CA

Identifiers

PMID33047659
PMCPMC7557680
OpenAlexW3091834514

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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.