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Multi-omics Study on the Pathogenesis of Malignant Transformation of Adenomyosis

A Multi-omics Study on the Pathogenesis of Malignant Transformation of Adenomyosis

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04010487
Enrollment
40
Registered
2019-07-08
Start date
2019-07-16
Completion date
2021-08-01
Last updated
2019-07-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adenomyosis, Ectopic Endometrial Tissue, Endometrial Cancer, Eutopic Endometrium, Genomics, Transcriptomics

Brief summary

This study is to explore the driving genes and the molecular mechanism of malignant transformation of adenomyosis. This study acquired the formalin fixed paraffin-embedded (FFPE) tissue of patients pathologically conformed endometrial carcinoma arising in adenomyosis (EC-AIA) treated at Peking Union Medical College Hospital from July 15, 2017 to July 15, 2019. The formalin fixed paraffin-embedded tissues from patients pathologically diagnosed with adenomyosis during this time period were also included as control specimens. The eutopic endometrium, normal adenomyosis tissue, and EC-AIA tissue were harvested from the FFPE tissue from patients with EC-AIA. The normal eutopic endometrium and normal adenomyosis tissue were obtained by laser microdissection. The driving genes and potential molecular mechanism of EC-AIA will be found by the technology of whole exome sequencing and transcriptomics (RNA-sequencing).

Interventions

GENETICwhole exome sequencing and RNA-sequencing

The specimens from adenomyosis, endometrial cancer, and eutopic endometrium will be tested by whole exome sequencing and RNA-sequencing

Sponsors

Lei Li
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Pathological confirmed diagnosis with atypical hyperplasia and malignant transformation of adenomyosis glandular epithelium (including endometrioid, serous and clear cell carcinoma), with or without concurrent endometrial carcinoma * Signed an approved informed consents

Exclusion criteria

* Not meeting all the inclusion criteria. * The formalin fixed paraffin-embedded (FFPE) tissue was not acquired at the required time period. * The patients enrolled had accompanied some other kinds of carcinoma (such as ovarian cancer, cervical cancer, primary peritoneal cancer). * Patients had cancer history of certain organ (such as colorectal cancer, gastric cancer, etc.)

Design outcomes

Primary

MeasureTime frameDescription
Frequencies of somatic driving mutationsOne yearThe differences of distributions and frequencies of somatic driving mutations will be compared between eutopic ectopic endometrium, and cancer tissues by whole exome sequencing
Frequencies of alteration of RNA expressionOne yearThe alteration of RNA expression, including mRNA, miRNA, and lncRNA will be compared between eutopic and ectopic endometrium, and cancer tissues by transcriptome sequencing

Countries

China

Contacts

Primary ContactLei Li, M.D.
lileigh@163.com+8613911988831

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026