Javascript must be enabled to continue!
Dissecting the molecular signatures underlying hybrid oncocytic tumors in Birt-Hogg-Dubé syndrome.
View through CrossRef
707 Background: Birt-Hogg-Dubé (BHD) syndrome is associated with an increased risk of renal tumors including the hybrid oncocytic tumors (HOT), renal oncocytoma (RO) and chromophobe renal cell carcinoma (CHRCC). HOT are known to exhibit morphological features overlapping between RO and CHRCC. The molecular underpinnings of HOT and the corresponding morphologic correlates remain poorly understood. Herein we aimed to understand the distinct molecular features underlying HOT and how the genomic phenotype differs from CHRCC. Methods: We performed next generation sequencing and single cell sequencing analysis to understand the clinico-pathologic aspects and tumor biology of HOT and CHRCC, including tumor development. This was followed by spatial transcriptome analysis of the distinct HOT tumor compartments, using nanoString GeoMX digital spatial profiler. The candidate biomarker expression was confirmed by immunohistochemistry (IHC) and RNA in situ hybridization (RNA-ISH), a unique gene expression visualization molecular technology. Results: We discovered unique gene expression signatures underlying the two distinct morphological patterns seen in HOT. FOXI1 and L1CAM show a striking mutually exclusive expression pattern in the two cellular populations seen within this tumor. The signature genes of RO like cells seen within HOT resembles the principal cells of the distal nephron seen in normal kidney; and the signature genes of the CHRCC like cells resembles the intercalated cells of the distal nephron. This suggests distal nephron as the cellular site of origin for HOT. We also nominated tumor specific biomarkers for HOT. Conclusions: We identified unique gene expression signatures which are definitional for HOT and nominated candidate diagnostic biomarkers to help distinguish HOT from other renal tumor subtypes with overlapping morphology. This finding would improve the diagnostic accuracy, assist familial genetic monitoring, and facilitate disease management.
American Society of Clinical Oncology (ASCO)
Title: Dissecting the molecular signatures underlying hybrid oncocytic tumors in Birt-Hogg-Dubé syndrome.
Description:
707 Background: Birt-Hogg-Dubé (BHD) syndrome is associated with an increased risk of renal tumors including the hybrid oncocytic tumors (HOT), renal oncocytoma (RO) and chromophobe renal cell carcinoma (CHRCC).
HOT are known to exhibit morphological features overlapping between RO and CHRCC.
The molecular underpinnings of HOT and the corresponding morphologic correlates remain poorly understood.
Herein we aimed to understand the distinct molecular features underlying HOT and how the genomic phenotype differs from CHRCC.
Methods: We performed next generation sequencing and single cell sequencing analysis to understand the clinico-pathologic aspects and tumor biology of HOT and CHRCC, including tumor development.
This was followed by spatial transcriptome analysis of the distinct HOT tumor compartments, using nanoString GeoMX digital spatial profiler.
The candidate biomarker expression was confirmed by immunohistochemistry (IHC) and RNA in situ hybridization (RNA-ISH), a unique gene expression visualization molecular technology.
Results: We discovered unique gene expression signatures underlying the two distinct morphological patterns seen in HOT.
FOXI1 and L1CAM show a striking mutually exclusive expression pattern in the two cellular populations seen within this tumor.
The signature genes of RO like cells seen within HOT resembles the principal cells of the distal nephron seen in normal kidney; and the signature genes of the CHRCC like cells resembles the intercalated cells of the distal nephron.
This suggests distal nephron as the cellular site of origin for HOT.
We also nominated tumor specific biomarkers for HOT.
Conclusions: We identified unique gene expression signatures which are definitional for HOT and nominated candidate diagnostic biomarkers to help distinguish HOT from other renal tumor subtypes with overlapping morphology.
This finding would improve the diagnostic accuracy, assist familial genetic monitoring, and facilitate disease management.
Related Results
Complex Collision Tumors: A Systematic Review
Complex Collision Tumors: A Systematic Review
Abstract
Introduction: A collision tumor consists of two distinct neoplastic components located within the same organ, separated by stromal tissue, without histological intermixing...
Implications of oncocytic change in papillary thyroid cancer
Implications of oncocytic change in papillary thyroid cancer
SummaryObjectiveAlthough the presence of oncocytic change in less than 75% of a tumour is not considered to indicate oncocytic variants of papillary thyroid carcinoma (PTC), we fre...
Oncocytic Variant of Adrenocortical Carcinoma: Case Report of a Rare Malignancy
Oncocytic Variant of Adrenocortical Carcinoma: Case Report of a Rare Malignancy
Adrenocortical carcinoma is a rare cancer. Oncocytic tumors of the adrenal gland are rarer. Most Oncocytic
Adrenal Neoplasms are benign and carry favourable prognosis. They are cla...
Are Cervical Ribs Indicators of Childhood Cancer? A Narrative Review
Are Cervical Ribs Indicators of Childhood Cancer? A Narrative Review
Abstract
A cervical rib (CR), also known as a supernumerary or extra rib, is an additional rib that forms above the first rib, resulting from the overgrowth of the transverse proce...
Differential Diagnosis of Neurogenic Thoracic Outlet Syndrome: A Review
Differential Diagnosis of Neurogenic Thoracic Outlet Syndrome: A Review
Abstract
Thoracic outlet syndrome (TOS) is a complex and often overlooked condition caused by the compression of neurovascular structures as they pass through the thoracic outlet. ...
Early Russian Reception of James Hogg (1830s)
Early Russian Reception of James Hogg (1830s)
The early Russian reception of the Scottish writer James Hogg (1770—1835), known in his homeland as an interpreter of folk ballads and the author of “The Confession of a Justified ...
Síndrome de birt-hogg-dubé associada a tumor renal híbrido em paciente feminina: relato de caso
Síndrome de birt-hogg-dubé associada a tumor renal híbrido em paciente feminina: relato de caso
A síndrome de Birt-Hogg-Dubé (BHD) é uma doença genética rara, autossômica dominante, causada por mutações no gene FLCN. Caracteriza-se pela tríade de fibrofoliculomas cutâneos, ci...
„Nicht schon wieder ein Pneumothorax“ – Fallbericht Birt-Hogg-Dubé-Syndrom
„Nicht schon wieder ein Pneumothorax“ – Fallbericht Birt-Hogg-Dubé-Syndrom
ZusammenfassungFalldarstellung eines 40-jährigen Patienten mit rezidivierend spontan auftretenden Pneumothoraces in der Vorgeschichte. Neben einer konservativen Versorgung eines Pn...

