scholarly journals Characterization of ductal carcinoma in situ cell lines established from breast tumor of a Singapore Chinese patient

2014 ◽  
Vol 14 (1) ◽  
Author(s):  
Jacklyn WY Yong ◽  
Meng Ling Choong ◽  
SiFang Wang ◽  
Yu Wang ◽  
Shermaine QY Lim ◽  
...  
BMC Cancer ◽  
2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Julia Samson ◽  
Magdalina Derlipanska ◽  
Oza Zaheed ◽  
Kellie Dean

Abstract Background Currently it is unclear how in situ breast cancer progresses to invasive disease; therefore, a better understanding of the events that occur during the transition to invasive carcinoma is warranted. Here we have conducted a detailed molecular and cellular characterization of two, patient-derived, ductal carcinoma in situ (DCIS) cell lines, ETCC-006 and ETCC-010. Methods Human DCIS cell lines, ETCC-006 and ETCC-010, were compared against a panel of cell lines including the immortalized, breast epithelial cell line, MCF10A, breast cancer cell lines, MCF7 and MDA-MB-231, and another DCIS line, MCF10DCIS.com. Cell morphology, hormone and HER2/ERBB2 receptor status, cell proliferation, survival, migration, anchorage-independent growth, indicators of EMT, cell signalling pathways and cell cycle proteins were examined using immunostaining, immunoblots, and quantitative, reverse transcriptase PCR (qRT-PCR), along with clonogenic, wound-closure and soft agar assays. RNA sequencing (RNAseq) was used to provide a transcriptomic profile. Results ETCC-006 and ETCC-010 cells displayed notable differences to another DCIS cell line, MCF10DCIS.com, in terms of morphology, steroid-receptor/HER status and markers of EMT. The ETCC cell lines lack ER/PR and HER, form colonies in clonogenic assays, have migratory capacity and are capable of anchorage-independent growth. Despite being isogenic, less than 30% of differentially expressed transcripts overlapped between the two lines, with enrichment in pathways involving receptor tyrosine kinases and DNA replication/cell cycle programs and in gene sets responsible for extracellular matrix organisation and ion transport. Conclusions For the first time, we provide a molecular and cellular characterization of two, patient-derived DCIS cell lines, ETCC-006 and ETCC-010, facilitating future investigations into the molecular basis of DCIS to invasive ductal carcinoma transition.


2011 ◽  
Vol 21 (9) ◽  
pp. 2011-2019 ◽  
Author(s):  
Habib Rahbar ◽  
Savannah C. Partridge ◽  
Peter R. Eby ◽  
Wendy B. DeMartini ◽  
Robert L. Gutierrez ◽  
...  

2012 ◽  
Vol 30 (6) ◽  
pp. 600-607 ◽  
Author(s):  
Min Yi ◽  
Funda Meric-Bernstam ◽  
Henry M. Kuerer ◽  
Elizabeth A. Mittendorf ◽  
Isabelle Bedrosian ◽  
...  

Purpose Prediction of patients at highest risk for ipsilateral breast tumor recurrence (IBTR) after local excision of ductal carcinoma in situ (DCIS) remains a clinical concern. The aim of our study was to evaluate a published nomogram from Memorial Sloan-Kettering Cancer Center to predict for risk of IBTR in patients with DCIS from our institution. Patients and Methods We retrospectively identified 794 patients with a diagnosis of DCIS who had undergone local excision from 1990 through 2007 at the MD Anderson Cancer Center (MDACC). Clinicopathologic factors and the performance of the Memorial Sloan-Kettering Cancer Center nomogram for prediction of IBTR were assessed for 734 patients who had complete data. Results There was a marked difference with respect to tumor grade, prevalence of necrosis, initial presentation, final margins, and receipt of endocrine therapy between the two cohorts. The biggest difference was that more patients received radiation in the MDACC cohort (75% at MDACC v 49% at MSKCC; P < .001). Follow-up time in the MDACC cohort was longer than in the MSKCC cohort (median 7.1 years v 5.6 years), and the recurrence rate was lower in the MDACC cohort (7.9% v 11%). The median 5-year probability of recurrence was 5%, and the median 10-year probability of recurrence was 7%. The nomogram for prediction of 5- and 10-year IBTR probabilities demonstrated imperfect calibration and discrimination, with a concordance index of 0.63. Conclusion Predictive models for IBTR in patients with DCIS who were treated with local excision are imperfect. Our current ability to accurately predict recurrence on the basis of clinical parameters alone is limited.


2011 ◽  
Vol 52 (4) ◽  
pp. 364-371 ◽  
Author(s):  
Yeon Ju Gwak ◽  
Hye Jung Kim ◽  
Jin Young Kwak ◽  
Sang Kwon Lee ◽  
Kyung Min Shin ◽  
...  

2009 ◽  
Vol 17 (6) ◽  
pp. 495-499 ◽  
Author(s):  
Mamatha Chivukula ◽  
Akosua Domfeh ◽  
Gloria Carter ◽  
George Tseng ◽  
David J. Dabbs

2014 ◽  
Vol 465 (3) ◽  
pp. 275-289 ◽  
Author(s):  
Mieke Van Bockstal ◽  
Kathleen Lambein ◽  
Hannelore Denys ◽  
Geert Braems ◽  
Ann Nuyts ◽  
...  

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