Characterization of NCC-RbC-51, an RB cell line isolated from a metastatic site.

Histochem Cell Biol

L&T Department of Ocular Pathology, Vision Research Foundation, Kamalnayan Bajaj Institute for Research in Vision and Ophthalmology, Old No 18, New No 41, College Road, Nungambakkam, Chennai, India.

Published: February 2020

Retinoblastoma (RB) is a childhood eye tumor, caused by the RB1 gene mutation. Since RB is a rapidly proliferating tumor, the patient presents with a Group-D/E tumor at the time of diagnosis. Enucleation is preferred in most unilateral cases to prevent metastasis. Various cell lines have been established to study the tumor's growth pattern and target the cancer cells. The commonly used cell lines are WERI-Rb-1 and Y79, both isolated from the primary tumor of RB. Cell lines established from the metastatic site of RB have not been characterized before. In this study, we have characterized NCC-RbC-51, derived from RB tumor to cervical lymph node site and investigated its potential to represent a highly aggressive and metastatic tumor. We compared the proliferative and invasive properties of NCC-RbC-51 with a cell line isolated from the primary site, WERI-Rb-1. NCC-RbC-51 had higher rates of proliferation and apoptosis and had better invasive ability. Copy number variation analysis and the pathways predicted from these show that the pathways altered in NCC-RbC-51 could contribute to its metastatic nature. In all, the results suggest that NCC-RbC-51, a cell line isolated from metastatic site, could be a potential model to study aggressive/invasive RB.

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00418-019-01832-1DOI Listing

Publication Analysis

Top Keywords

ncc-rbc-51 cell
12
cell isolated
12
metastatic site
12
cell lines
12
isolated metastatic
8
lines established
8
isolated primary
8
cell
6
tumor
6
metastatic
5

Similar Publications

Retinoblastoma (RB) is a rare ocular cancer seen in children that counts for approximately 3% of all childhood cancers. It is found that mutation in RB1, a tumour Suppressor Gene on chromosome 13 as the cause of malignancy. Retinoblastoma protein is the target for ceramide to cause apoptosis.

View Article and Find Full Text PDF

Serum exosomal miRNA as biomarkers for Retinoblastoma.

Exp Eye Res

October 2020

L & T Department of Ocular Pathology, Vision Research Foundation, Kamalnayan Bajaj Institute for Research in Vision and Ophthalmology, Chennai, India; Radheshyam Kanoi Stem Cell Laboratory, Vision Research Foundation, Kamalnayan Bajaj Institute for Research in Vision and Ophthalmology, Chennai, India. Electronic address:

Retinoblastoma (RB) is a childhood eye tumor, caused by RB1 mutation. Though diagnosing RB is easier, prognosticating RB is limited to examining the patient under anesthesia and imaging technique. The aim of the study is to find exosomal miRNA biomarkers to prognosticate RB.

View Article and Find Full Text PDF

Gene expression profiling of tumor stroma interactions in retinoblastoma.

Exp Eye Res

August 2020

Larsen & Toubro Department of Ocular Pathology, Vision Research Foundation, Kamalnayan Bajaj Institute for Research in Vision and Ophthalmology, Chennai, 600006, Tamil Nadu, India; School of Medicine, Institute for Innovation in Mental and Physical Health and Clinical Translation (IMPACT), Deakin University, Geelong, 3216, VIC, Australia. Electronic address:

Article Synopsis
  • Scientists wanted to understand how retinoblastoma (a type of eye cancer) cells interact with nearby cells, specifically bone marrow cells, to see what changes in their genes.
  • They grew two different retinoblastoma cell types with bone marrow cells in the lab and looked at how the genes were expressed using special technology.
  • They found many genes that changed due to these interactions, which might help scientists develop new treatments for retinoblastoma in the future.
View Article and Find Full Text PDF

Characterization of NCC-RbC-51, an RB cell line isolated from a metastatic site.

Histochem Cell Biol

February 2020

L&T Department of Ocular Pathology, Vision Research Foundation, Kamalnayan Bajaj Institute for Research in Vision and Ophthalmology, Old No 18, New No 41, College Road, Nungambakkam, Chennai, India.

Retinoblastoma (RB) is a childhood eye tumor, caused by the RB1 gene mutation. Since RB is a rapidly proliferating tumor, the patient presents with a Group-D/E tumor at the time of diagnosis. Enucleation is preferred in most unilateral cases to prevent metastasis.

View Article and Find Full Text PDF

Background: Lactate dehydrogenase (LD), a tetrameric product of the genes LDHA and LDHB, may be increased in sera of cancer patients. A variant isoenzyme with electrophoretic mobility between LD2 and LD3 (LD2ex) has been described in patients, but its molecular nature is largely unknown.

Methods: A newly established retinoblastoma cell line, NCC-RbC-51 (R51), showed an isoenzyme pattern with only two bands, LD1 and LD2ex.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!