Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Abstract 1399: Ex-vivo targeting of urothelial carcinomas by fluorescent pHLIP imaging agents

View through CrossRef
Abstract Introduction: The detection of urothelial carcinomas of the bladder and upper tract is not satisfactory. Incomplete findings by contemporary imaging modalities provide a challenge in patient care, so there is a definitive need to improve diagnosis and treatment methods for urothelial carcinomas. Experimental procedures: ICG (indocyanine green) near infrared fluorescent (NIRF) dyes were conjugated with a pH-Low Insertion Peptide (pHLIP®), which senses and targets the acidity at the surfaces of cancer cells. In a few cases IR800 pHLIP® was used. Urinary neoplasm (kidney, ureter and bladder) specimens obtained through radical surgery were irrigated and incubated ex-vivo with ICG pHLIP® followed by fluorescence imaging. Pathology findings were correlated with the ICG pHLIP® NIRF imaging. Results: In the upper urothelial tract, nine of ten patients with nephroureterectomy had urothelial carcinomas (UTUC). Eighteen (100%) malignant lesions were found in NIRF imaging. Only thirteen (72%) of malignant lesions were found under white light macroscopic examination. ICG pHLIP® NIRF imaging gave a 28% increase in diagnosis of UTUC in ex-vivo specimens. There was no non-specific uptake in the non-tumoral tissue. The ICG pHLIP® imaging agent identified malignant upper tract urothelial lesions with 100% specificity and sensitivity. In the lower urinary tract, thirty-eight radical cystectomy specimens were incubated with pHLIP® conjugated with one of the NIRF dyes (ICG or IR800). In the thirty-eight bladders, eighty-one lesions were identified using fluorescent pHLIP®(specificity (97%) and sensitivity (100%)). White light cystoscopy did not detect 20.5% of lesions identified under NIRF cystoscopy (p<.001). Normal tissue did not show any uptake by the construct; however, entrapment of the dye in the necrotic tumor bed was noted. All regions showing the NIRF signal of pHLIP® were confirmed by standard pathological analysis. Conclusions: The ICG pHLIP® NIRF revealed additional lesions not seen with white light ex-vivo cystoscopy or preoperative ureteroscopy. pHLIP® based agents promise to improve diagnostic accuracy for urothelial carcinomas and may enable targeted treatment. Citation Format: Borivoj Golijanin, Anna Moshnikova, Donald M. Engelman, Oleg A. Andreev, Yana K. Reshetnyak, Ali Amin, Dragan Golijanin. Ex-vivo targeting of urothelial carcinomas by fluorescent pHLIP imaging agents [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2019; 2019 Mar 29-Apr 3; Atlanta, GA. Philadelphia (PA): AACR; Cancer Res 2019;79(13 Suppl):Abstract nr 1399.
Title: Abstract 1399: Ex-vivo targeting of urothelial carcinomas by fluorescent pHLIP imaging agents
Description:
Abstract Introduction: The detection of urothelial carcinomas of the bladder and upper tract is not satisfactory.
Incomplete findings by contemporary imaging modalities provide a challenge in patient care, so there is a definitive need to improve diagnosis and treatment methods for urothelial carcinomas.
Experimental procedures: ICG (indocyanine green) near infrared fluorescent (NIRF) dyes were conjugated with a pH-Low Insertion Peptide (pHLIP®), which senses and targets the acidity at the surfaces of cancer cells.
In a few cases IR800 pHLIP® was used.
Urinary neoplasm (kidney, ureter and bladder) specimens obtained through radical surgery were irrigated and incubated ex-vivo with ICG pHLIP® followed by fluorescence imaging.
Pathology findings were correlated with the ICG pHLIP® NIRF imaging.
Results: In the upper urothelial tract, nine of ten patients with nephroureterectomy had urothelial carcinomas (UTUC).
Eighteen (100%) malignant lesions were found in NIRF imaging.
Only thirteen (72%) of malignant lesions were found under white light macroscopic examination.
ICG pHLIP® NIRF imaging gave a 28% increase in diagnosis of UTUC in ex-vivo specimens.
There was no non-specific uptake in the non-tumoral tissue.
The ICG pHLIP® imaging agent identified malignant upper tract urothelial lesions with 100% specificity and sensitivity.
In the lower urinary tract, thirty-eight radical cystectomy specimens were incubated with pHLIP® conjugated with one of the NIRF dyes (ICG or IR800).
In the thirty-eight bladders, eighty-one lesions were identified using fluorescent pHLIP®(specificity (97%) and sensitivity (100%)).
White light cystoscopy did not detect 20.
5% of lesions identified under NIRF cystoscopy (p<.
001).
Normal tissue did not show any uptake by the construct; however, entrapment of the dye in the necrotic tumor bed was noted.
All regions showing the NIRF signal of pHLIP® were confirmed by standard pathological analysis.
Conclusions: The ICG pHLIP® NIRF revealed additional lesions not seen with white light ex-vivo cystoscopy or preoperative ureteroscopy.
pHLIP® based agents promise to improve diagnostic accuracy for urothelial carcinomas and may enable targeted treatment.
Citation Format: Borivoj Golijanin, Anna Moshnikova, Donald M.
Engelman, Oleg A.
Andreev, Yana K.
Reshetnyak, Ali Amin, Dragan Golijanin.
Ex-vivo targeting of urothelial carcinomas by fluorescent pHLIP imaging agents [abstract].
In: Proceedings of the American Association for Cancer Research Annual Meeting 2019; 2019 Mar 29-Apr 3; Atlanta, GA.
Philadelphia (PA): AACR; Cancer Res 2019;79(13 Suppl):Abstract nr 1399.

Related Results

Targeting bladder urothelial carcinoma with pHLIP-ICG and inhibition of urothelial cancer cell proliferation by pHLIP-amanitin
Targeting bladder urothelial carcinoma with pHLIP-ICG and inhibition of urothelial cancer cell proliferation by pHLIP-amanitin
Acidity is a useful biomarker for the targeting of metabolically active cells in tumors. pH Low Insertion Peptides (pHLIPs) sense the pH at the surfaces of tumor cells and can faci...
Abstract 4250: pHLIP® technology for imaging acidic tumors
Abstract 4250: pHLIP® technology for imaging acidic tumors
Abstract Introduction: Extracellular acidosis promotes tumor development, progression and invasiveness. A combination of effects acidifies tumor cell ...
Abstract 6759: Antigen-pHLIP for tumor treatment
Abstract 6759: Antigen-pHLIP for tumor treatment
Abstract Targeted antigen delivery allows activation of the immune system to kill tumor cells. Among the immunogenic epitopes widely investigated is α-Gal, since hum...
Acid-driven immune suppression by pHLIP-fused PD-L1 under inflammatory conditions
Acid-driven immune suppression by pHLIP-fused PD-L1 under inflammatory conditions
Abstract Programmed cell death–ligand 1 (PD-L1)/PD-1 axis is crucial for maintenance of immune homeostasis and its impairment partially accounts for the pathogenesis of inf...
SALL4 Expression in Urothelial Carcinoma of Urinary Bladder; aTissue Microarray Analysis
SALL4 Expression in Urothelial Carcinoma of Urinary Bladder; aTissue Microarray Analysis
Sal-like protein 4 (SALL4) is a cellular pluripotent embryonic nuclear factor that has been a useful immunohistochemistry marker for germ-cell tumors. Our understanding of SALL4 ex...
Breast Carcinoma within Fibroadenoma: A Systematic Review
Breast Carcinoma within Fibroadenoma: A Systematic Review
Abstract Introduction Fibroadenoma is the most common benign breast lesion; however, it carries a potential risk of malignant transformation. This systematic review provides an ove...
Immunohistochemistry in ocular carcinomas
Immunohistochemistry in ocular carcinomas
Background:  The distinction between ocular sebaceous carcinoma, poorly differentiated ocular squamous cell carcinoma and ocular basal cell carcinoma can be challenging. An appropr...

Back to Top