Evidence map›Paper›PMID 30212483›Full record

Trial reportPloS one2018

Prevalence and spectrum of AKT1, PIK3CA, PTEN and TP53 somatic mutations in Chinese breast cancer patients.

Guoli Li, Xinwu Guo, Ming Chen, Lili Tang, Hui Jiang, Julia X Day, Yueliang Xie, Limin Peng, Xunxun Xu, Jinliang Li and 4 more

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 12% 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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Pooled it
  2. Observational
  3. Article
  4. Article
  5. Review
  6. Precision therapy in metastatic breast cancer: the current landscape of molecular alteration-based therapies.Translational breast cancer research : a journal focusing on translational research in breast cancer · 2025
    Review
  7. Precision diagnosis and treatment of PI3K/AKT/PTEN signaling pathway in HR-positive advanced breast cancer: perspectives from Chinese experts.Translational breast cancer research : a journal focusing on translational research in breast cancer · 2025
    Review
  8. Article
  9. Article
  10. Article
  11. Comparison ofJCO precision oncology · 2022
    Article
  12. Loss of PTEN Expression, PIK3CA Mutations, and Breast Cancer Survival in the Nurses' Health Studies.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2022
    Article
  13. Current oncology (Toronto, Ont.) · 2022
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article
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

14 authors at 1 institution in 1 country.

Guoli LiSchool of Life Sciences, Central South University, Changsha, Hunan, China.
Xinwu GuoSanway Gene Technology Inc., Changsha, Hunan, China.
Ming ChenSanway Gene Technology Inc., Changsha, Hunan, China.
Lili TangDepartment of Breast Surgery, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Hui JiangSchool of Life Sciences, Central South University, Changsha, Hunan, China.
Julia X DaySanway Gene Technology Inc., Changsha, Hunan, China.
Yueliang XieSchool of Life Sciences, Central South University, Changsha, Hunan, China.
Limin PengSanway Gene Technology Inc., Changsha, Hunan, China.
Xunxun XuSanway Gene Technology Inc., Changsha, Hunan, China.
Jinliang LiSanway Gene Technology Inc., Changsha, Hunan, China.
Shouman WangDepartment of Breast Surgery, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Zhi XiaoDepartment of Breast Surgery, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Lizhong DaiSanway Gene Technology Inc., Changsha, Hunan, China.
Jun WangSchool of Life Sciences, Central South University, Changsha, Hunan, China.ORCID 0000-0001-8008-4563
Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer, one of the most frequently occurring cancers worldwide, is the leading cause of cancer-related death among women. AKT1, PIK3CA, PTEN and TP53 mutations were common observed in breast cancer representing potential clinical biomarkers for cancer classification and treatment. A comprehensive knowledge of AKT1, PIK3CA, PTEN and TP53 mutations in breast cancer was still insufficient in Chinese population. In this study, the complete coding regions and exon-intron boundaries of AKT1, PIK3CA, PTEN and TP53 genes were sequenced in paired breast tumor and normal tissues from 313 Chinese breast cancer patients using microfluidic PCR-based target enrichment and next-generation sequencing technology. Total 120 somatic mutations were identified in 190 of the 313 patients (60.7%), with the mutation frequency of AKT1 as 3.2%, PIK3CA as 36.4%, PTEN as 4.8%, and TP53 as 33.9%. Among these mutations, 1 in PIK3CA (p.I69N), 3 in PTEN (p.K62X, c.635-12_636delTTAACCATGCAGAT and p.N340IfsTer4) and 5 in TP53 (p.Q136AfsTer5, p.K139_P142del, p.Y234dup, p.V274LfsTer31 and p.N310TfsTer35) were novel. Notably, PIK3CA somatic mutations were significantly associated with ER-positive or PR-positive tumors. TP53 somatic mutations were significantly associated with ER-negative, PR-negative, HER2-positive, BRCA1 mutation, Ki67 high expression and basal-like tumors. Our findings provided a comprehensive mutation profiling of AKT1, PIK3CA, PTEN and TP53 genes in Chinese breast cancer patients, which have potential implications in clinical management.

Indexed as

AdultAgedAged, 80 and overAsian PeopleBreast NeoplasmsChinaClass I Phosphatidylinositol 3-KinasesFemaleHumansMiddle AgedProto-Oncogene Proteins c-aktPTEN PhosphohydrolaseTumor Suppressor Protein p53AKT1 protein, humanClass I Phosphatidylinositol 3-KinasesPIK3CA protein, humanProto-Oncogene Proteins c-aktPTEN PhosphohydrolasePTEN protein, humanTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID30212483
PMCPMC6136723
OpenAlexW2892334526

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.