Survivin-Sodium Iodide Symporter Reporter as a Non-Invasive Diagnostic Marker to Differentiate Uterine Leiomyosarcoma from Leiomyoma

Qiwei Yang & Ayman Al-Hendy et al. · 2023-12-13

Leiomyosarcoma (LMS) has been challenging to diagnose because of limitations in clinical and radiographic predictors, as well as the lack of reliable serum or urinary biomarkers. Most uterine masses consist of benign leiomyoma (LM). However, it is currently a significant challenge in gynecology practice to differentiate LMS from LM. This inability poses grave consequences for patients, leading to a high number of unnecessary hysterectomies, infertility, and other major morbidities and possible mortalities. This study aimed to evaluate the use of Survivin-Sodium iodide symporter (Ad-Sur-NIS) as a reporter gene biomarker to differentiate malignant LMS from benign LM by using an F18-NaBF4 PET/CT scan. The PET/CT scan images showed a significantly increased radiotracer uptake and a decreased radiotracer decay attributable to the higher abundance of Ad-Sur-NIS in the LMS tumors compared to LM (p < 0.05). An excellent safety profile was observed, with no pathological or metabolic differences detected in Ad-Sur-NIS-treated animal versus the vehicle control. Ad-Sur-NIS as a PET scan reporter is a promising imaging biomarker that can differentiate uterine LMS from LM using F18-NaBF4 as a radiotracer. As a new diagnostic method, the F18 NaBF4 PET/CT scan can provide a much-needed tool in clinical practices to effectively triage women with suspicious uterine masses and avoid unnecessary invasive interventions.

Journal
Cells
Funding
Pathological reprogramming of the m6A epitranscriptome in uterine fibroidsInvestigating the effectiveness of COVID-19 testing choices, community engagement, and culturally-embedded mHealth literacy delivery in a medically-underserved, community-based sampleInvestigating the effectiveness of COVID-19 testing choices, community engagement, and culturally-embedded mHealth literacy delivery in a medically-underserved, community-based sampleAdministrative CoreMechanisms of actions(s) of simvastatin in uterine leiomyomaMechanisms of actions(s) of simvastatin in uterine leiomyomaHypovitaminosis D promotes MED12-associated genomic instability in uterine fibroidsAdministrative CorePathological reprogramming of the m6A epitranscriptome in uterine fibroidsHypovitaminosis D promotes MED12-associated genomic instability in uterine fibroidsUniversity of Illinois at Chicago Grant Proof of concept 2020University of Illinois at Chicago Grant RO1 HD094378University of Illinois at Chicago Grant RO1 ES028615Administrative CoreUniversity of Illinois at Chicago Grant RO1 HD094380University of Illinois at Chicago Grant RO1 HD106285National Institutes of Health (NIH) Grant Proof of concept 2020National Institutes of Health Grant RO1 HD094378National Institutes of Health Grant RO1 ES028615Administrative CoreNational Institutes of Health (NIH) Grant RO1 HD094380National Institutes of Health Grant RO1 HD106285

NIEHS NIH HHS

R01 ES028615

NIH HHS

MD007602

NICHD NIH HHS

R01 HD094380

NIMHD NIH HHS

U54 MD007602

NICHD NIH HHS

R01 HD106285

NICHD NIH HHS

R01 HD094378

University of Illinois at Chicago

U54 MD007602

National Institutes of Health (NIH)

U54 MD007602