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Transcriptome of Breast Tumors With Different Amplification Status of the Long Arm of Chromosome 8
- Source :
- Anticancer Research. 41:187-195
- Publication Year :
- 2021
- Publisher :
- Anticancer Research USA Inc., 2021.
-
Abstract
- Background Amplification of chromosome 8q with locus 8q24 is the most common copy number aberration, and is associated with tumour progression and chemoresistance. Materials and methods The study used paired samples of biopsy and surgical material from 60 patients with breast cancer. The amplification status of 8q was determined using a CytoScan HD Array microarray; complete transcriptomic analysis was performed using a Human Clariom S Assays microarray (Affymetrix, USA). Results It was shown that in 65% of cases, amplification of 8q was preserved in the tumour after neoadjuvant chemotherapy (NAC). NAC significantly enhanced the heterogeneity of the transcriptome between tumours with and without amplification of 8q. Compared with a good response, a poor response to NAC also led to increased heterogeneity of the transcriptome of residual tumours. Eight differentially expressed genes of patients with different amplification status of 8q before and after NAC overlapped. Conclusion Amplification of 8q leads to a significant shift in the level of transcription of a large number of genes after exposure to chemotherapy.
- Subjects :
- Adult
Cancer Research
Microarray
medicine.medical_treatment
Breast Neoplasms
Locus (genetics)
Biology
Transcriptome
Young Adult
03 medical and health sciences
0302 clinical medicine
Breast cancer
Gene Frequency
Biopsy
Biomarkers, Tumor
medicine
Humans
Gene
Aged
Neoplasm Staging
Chemotherapy
medicine.diagnostic_test
Gene Expression Profiling
Gene Amplification
Computational Biology
Chromosome
General Medicine
Middle Aged
medicine.disease
Combined Modality Therapy
Gene Expression Regulation, Neoplastic
Oncology
030220 oncology & carcinogenesis
Cancer research
Female
Chromosomes, Human, Pair 8
Subjects
Details
- ISSN :
- 17917530 and 02507005
- Volume :
- 41
- Database :
- OpenAIRE
- Journal :
- Anticancer Research
- Accession number :
- edsair.doi.dedup.....698f38142d0a72234cecf081c92b190a