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Light condition | Overexpressed genes after irradiation | Possible cancers affected |
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Blue | BUB1B | Brain and lung cancer |
ERCC5 | Ovarian cancer |
FANCD2 | Breast cancer and Fanconi anemia |
MSR1 | Prostate cancer and Barrett’s esophagus/esophageal adenocarcinoma |
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Green | ANTXR2 | Hyaline fibromatosis syndrome and hyalinosis, inherited systemically (its related pathways are infectious disease and uptake and actions of bacterial toxins) |
BUB1B | Brain and lung cancers |
DIS3L2 | Perlman syndrome and Wilms’ tumor susceptibility-5 |
EPCAM | Endometrial cancer, biliary tract cancer, and skin cancer |
ESCO2 | Roberts syndrome and SC phocomelia syndrome |
EPHB2 | Prostate cancer/brain cancer susceptibility, somatic and prostate cancer |
EXT1 | Chondrosarcoma and exostoses, multiple, type 1 |
FANCD2 | Breast cancer and Fanconi anemia |
KIT | Endometrial cancer as a gastrointestinal stromal tumor |
MSR1 | Prostate cancer and Barrett’s esophagus/esophageal adenocarcinoma |
NF1 | Neurofibromatosis-Noonan syndrome and neurofibromatosis, type 1 |
RET | Multiple endocrine neoplasia iia and medullary thyroid carcinoma, familial |
TSC1 | Tuberous sclerosis-1 and lymphangioleiomyomatosis |
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Red | BUB1B | Brain and lung cancer |
DIS3L2 | Perlman syndrome and Wilms’ tumor susceptibility-5 |
FANCB | Fanconi anemia, complementation group B, and Fanconi anemia, complementation group A |
FANCD2 | Breast cancer and Fanconi anemia |
KIT | Endometrial cancer as a gastrointestinal stromal tumor |
MSR1 | Prostate cancer and Barrett’s esophagus/esophageal adenocarcinoma |
POLE | FILS syndrome and colorectal cancer 12 |
POLH | Xeroderma pigmentosum, variant type and POHL-related xeroderma pigmentosum |
RET | Multiple endocrine neoplasia iia and medullary thyroid carcinoma, familial |
SUFU | Medulloblastoma and basal cell nevus syndrome |
TMC8 | Epidermodysplasia verruciformis and superficial mycosis |
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