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Immunohistochemical Expression of Epithelial Cell Adhesion Molecule (EpCAM) in Epithelial Ovarian Carcinoma

S

Sohag University

Status

Enrolling

Conditions

Ovarian Carcinoma

Study type

Observational

Funder types

Other

Identifiers

NCT05576519
Soh-Med-22-09-15

Details and patient eligibility

About

Cancer stem cells (CSCs) can undergo self-renewal and differentiation. EpCAM is a 40-kDa type I transmembrane glycoprotein composed of a large extracellular domain, one transmembrane region, and a small intracellular domain of 26 amino acids. Recent insights revealed that it is involved in promoting cancer cell proliferation, migration, and invasiveness. It is used as a diagnostic and prognostic marker. EpCAM has also recently been identified as a marker for CSCs.

Full description

Ovarian carcinoma is one of most frequent cancer in women worldwide. Epithelial ovarian carcinoma is a group of neoplasms with different histologic pictures. Serous carcinoma is the most common type.

Cancer stem cells (CSCs) can undergo self-renewal and differentiation. EpCAM is a 40-kDa type I transmembrane glycoprotein composed of a large extracellular domain, one transmembrane region, and a small intracellular domain of 26 amino acids. It is abundantly expressed by the majority of human epithelial carcinomas, including colorectal, breast, lung, prostate, ovarian, and endometrial cancers. it is overexpressed in various neoplasms. Recent insights revealed that it is involved in promoting cancer cell proliferation, migration, and invasiveness. It is used as a diagnostic and prognostic marker. EpCAM has also recently been identified as a marker for CSCs.

Enrollment

50 estimated patients

Sex

Female

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with epithelial ovarian carcinoma and underwent surgery

Exclusion criteria

    • Cases received pre-operative chemotherapy or radiotherapy.
  • Cases with insufficient clinical data.

Trial contacts and locations

2

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Central trial contact

Nagwa Ahmed, Lecture

Data sourced from clinicaltrials.gov

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