Skip to search boxSkip to navigationSkip to main content

Molecular Bio-Imaging Probe for Non-Invasive Differentiation Between Human Leiomyoma Versus Leiomyosarcoma

  • Shahinaz Shalaby
    ,
  • Mostafa Khater
    ,
  • Archana Laknaur
    ,
  • ,
  • Ayman Al-Hendy(corresponding author)
*Corresponding author for this work
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Leiomyosarcoma is the most frequent subtype of the deadly uterine sarcoma and shares many common clinical grounds with leiomyoma, which is in turn the most common solid benign uterine neoplasm. With the recent progress in minimally invasive techniques for managing leiomyomas, accurate preoperative diagnosis of uterine masses has become the most important selection criterion for the safest therapeutic option. Therefore, different imaging modalities would be playing a key role in management of uterine masses. Testing for a sarcoma-specific promoter that expresses its downstream reporter gene only in leiomyosarcoma and not in leiomyoma or healthy uterine tissue. Adenoviral vectors were utilized both in vitro and in vivo to test the specificity of the promoters. Quantitative studies of downstream gene expression of these promoters was carried out both in vitro and in vivo. Our data indicated that human leiomyosarcoma cells highly expressed the reporter gene downstream to survivin promoter (Ad-SUR-LUC) when compared with benign leiomyoma or normal cells (p value of 0.05). Our study suggested that survivin is the unique promoter capable of distinguishing between the deadly sarcoma and the benign counterparts.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 644-654 (11 pages)

Journal (Volume, Issue Number)

Reproductive Sciences (Volume 27, Issue 2)

Publication milestones

  • Published - 02/01/2020

Publication status

Published - 02/01/2020

ISSN

1933-7191

Publication IDs

  • Scopus: 85079818434
  • PubMed: 31925772

Publication metrics

Metrics

SciVal
citations
1
SciVal
FWCI
0.64
SciVal
Author count
5
SciVal
Paper percentile
68
Fractional count
2
Fractional count
0.40
Fractional count
3
Fractional count
0.60
Fractional count
2
Fractional count
1
Scopus
citations

PlumX, opens in new tab

Citation count
6
Captures
10

Funding Details

This study was funded by the National Institute of Health (R01 ES 028615–01, R01HD 087417, R01 HD 094378, R01 HD 094380).
FundersFunding numbers
National Institutes of Health, National Cancer Institute
R01 HD 094380, R01 HD 094378, R01 ES 028615–01, R01HD 087417
NICHD
R01HD087417