Table 1.
Specific Chromosome Abnormalities Involved in Tumorigenesis and Cancer Recurrence
| Cancer Type | Chromosome Abnormalities | Characteristic | Reference |
|---|---|---|---|
| Neural lineage cancers | recurrent chr7 gain | common feature | 53 |
| Glioblastoma | chr7 gain and 10 loss | without IDH mutations | 53,54 |
| chr19q gain and 1p loss | with IDH mutations | 55 | |
| Neuroblastoma | chr2p and 17q gain; chr1p and 11q deletion | common feature | 55 |
| focal loss of chr7q14.1 and chr14q11.2 | a predictive indicator for poorer prognosis | 55 | |
| Low-grade glioma | chr1p and 19q deletion | responsive to chemoradiotherapy | 53,57 |
| Head and neck squamous cell carcinoma | chr3q, 5p, 8p, and 11q gain | tumorigenesis | 60,61 |
| chr3 (3q26-29) gain | a predictive indicator for poorer prognosis | 58 | |
| Oral squamous cell carcinoma | chr11q22.1-q22.2 amplification | correlation with recurrence and radiotherapy | 59 |
| Lung squamous cell carcinoma | chr3q gain and 3p loss | common feature | 53 |
| Lung adenocarcinoma | chr1q gain | cancer feature | 53,63 |
| chr7p gain | correlation with prognosis in patients with EGFR mutation | 67 | |
| Breast cancer | chr1q21.3 amplification | relation with recurrence | 68 |
| chr16q loss | low-grade breast neoplasia | 69 | |
| Few copy number variations (CNVs) in chr17 | relation with male breast cancer | 70 | |
| Gastrointestinal cancer | chr3q and 8q amplifications | triple-negative breast cancer (TNBC) with lung metastasis | 71 |
| Gastrointestinal tract adenocarcinoma (GIAC) | chr13q gain | common feature | 53 |
| Esophageal squamous cell carcinoma (ESCC) | chr9p21.3 and 2q35 loss; and chr2q31.2, 3q27, 5p15.33, 7q22.1, 8q24, 8p11.23, 11q13.3 gain | common feature | 74 |
| Adrenocortical carcinoma | chr19 gain | relation with stage III/IV | 75 |
| chr5, 12, 19, and 20 gain; and chr1, 10, 18, and 22 loss | common feature | 75,76 | |
| chr11p, 17p loss, and 9q gain | pediatric adrenocortical carcinoma | 77,78 | |
| Clear cell renal cell carcinoma | chr3p loss and 9q gain | common feature | 79, 80, 81 |
| Hematologic malignancies | chr20q loss | common feature | 82,83 |
| Lymphoid neoplasms | chr1p36 loss | diffuse follicular lymphoma | 84 |
| Burkitt-like lymphoma | chr11q aberration | common feature | 84 |
| Myelodysplastic syndromes | chr5q loss | common feature | 84 |
| B cell acute lymphoblastic leukemia | chr21 gain | common feature | 84 |
| B cell precursor acute lymphoblastic leukemia (B-ALL) | chr21 gain | relation with 12q abnormalities in B-ALL | 85 |
| Testicular germ cell cancers | chr12p gain | common feature | 87 |
| Ovarian cancer and endometrial cancers | chr1q gain | common feature | 53 |
| Prostate cancer | chr16p13.3 gain | an elevated risk of distant metastases | 88 |
| chr8q24 variation | a major contributor to prostate cancer | 89 |