Table 1.
Condition | Number of Patients | SA-β-Gal Localization | Results | Reference |
---|---|---|---|---|
Primary ovarian cancer | 11 | Cells of ovarian cancer not subject to chemotherapy | SA-β-gal activity was detected in 100% of cases of primary ovarian cancer | [24] |
Epithelial ovarian adenocarcinoma | 40 | Healthy tissues and epithelial ovarian adenocarcinoma | SA-β-gal activity in tumor tissues is 50% higher than in healthy tissues | [25] |
Colon adenocarcinoma | 7 | Colon adenocarcinoma tissue | SA-β-gal activity in adenocarcinoma tissues is 2 times higher than normal | [26] |
Colon adenoma and untreated invasive carcinoma | 23 | Senescent cells within neoplastic epithelial areas of manifest colorectal carcinomas | SA-β-gal activity was found in 8 out of 12 adenomas, 1 of out 6 invasive carcinomas, 0 out of 5 normal crypt mucosa tissues | [27] |
Colon adenoma | 59 | Cells of colon adenomas | A strong correlation between SA-β-gal staining and senescence immunohistochemical markers | [28] |
Glioma | 23 | Cells of malignant glial tumors | The greatest increase in the activity of β-galactosidase was in anaplastic oligodendroglioma; in other glial tumors, it was also higher than in meningiomas and metastatic tumors | [21] |
Glioma | 5 | Tumor-associated brain endothelial cells | SA-β-gal activity was detected in glioma tissue cells, while normal brain tissue was negative | [29] |
Breast cancer, fibroadenoma, fibrocystic disease |
18 | Carcinomas, fibrocystic, fibroadenomatous tissues | SA-β-gal activity was normal in fibroadenoma cells, increased in fibrocystic cells, and maximum level was observed in breast cancer cells | [26] |
Breast cancer | 56 | Tissues of treated and untreated breast tumors | SA-β-gal activity was detected in 15 of 36 tumors. Tumor sections of patients who had not received chemotherapy expressed SA-β-gal in 2 of 20 cases | [30] |
Prostate cancer, benign prostatic hyperplasia, high-grade prostatic intraepithelial neoplasia |
124 | Human prostate epithelial cells | High expression of SA-β-gal was observed in 37% of primary cancer specimens, 72% of high-grade prostatic intraepithelial neoplasia samples, and 13% of benign tissues | [31] |
Benign prostatic hyperplasia | 43 | Human prostate epithelial cells of hypertrophied tissues | SA-β-gal activity was detected in 17 out of 43 specimens. Prostate epithelial cells expressed SA-β-gal in patients with more pronounced prostate enlargement weighing more than 55 g, while the senescent cells were absent in prostate cells weighing less than 55 g | [32] |
Prostate cancer | 126 | Senescent prostate cancer cells | GLB1 staining was expressed at higher levels in prostate samples treated with androgen deprivation | [33] |
Chronic hepatitis C, hepatocellular carcinoma | 57 | Replicating cells in normal liver, liver with chronic hepatitis C and hepatocellular carcinomas | In normal liver tissue, SA-β-gal activity can be detected in 20% of cases. SA-β-gal was expressed in 60% of hepatocellular carcinoma samples and in 50% of samples with hepatitis C | [34] |
Chronic viral hepatitis | 20 | Tissues of liver with chronic viral hepatitis B, chronic viral hepatitis C, and normal liver | The SA-β-gal activity was frequently detected in periportal or periseptal hepatocytes of liver cirrhosis and focally in chronic hepatitis irrespective of type B or type C infection, while the enzyme activity was extremely weak in normal livers | [35] |
Hepatocellular carcinoma | 95 | Cancer cells | High SA-β-gal activity in tumor and low SA-β-gal activity in non-tumor tissues | [36] |
Lung Cancer | 6 | Tumor cells treated with chemotherapy and radiation | The enzyme was not detected in samples from patients who did not receive chemotherapy. SA-β-gal expression elevated in tissues after neoadjuvant chemotherapy | [37] |
Melanocytic naevi | 23 | Tissues of congenital naevi | Human naevi, largely growth-arrested neoplastic lesions, are positive for the senescence marker SA-β-gal | [38] |
Melanocytic naevi | 17 | Adult nevi cells | Every specimen evaluated showed varying degrees of positivity at the optimal pH 4, none of the specimens showed staining at pH 6 | [39] |
Knee osteoarthritis | 50 | Chondrocytes in articular cartilage | SA-β-gal staining was found in a subset of chondrocytes close to the lesion site of mild, moderate, and severely altered knee cartilage with osteoarthritis. No SA-β-gal staining was observed in normal articular cartilage samples | [40] |
Atherosclerosis | 3 | Atherosclerotic aorta | The aortic endothelium cells overlying atherosclerotic plaques were SA-β-gal-positive. The endothelium covering nearby regions of relatively normal aorta was SA-β-gal-negative |
[41] |
Gastric cancer | 13 | Gastric cancer cells, peritoneum metastatic cells | The SA-β-gal content in the tumor was high. SA-β-gal allowed locating peritoneal metastases | [42] |
Intraductal papillary mucinous neoplasm of the pancreas | 39 | Neoplasms with low-, intermediate- and high-grade dysplasia, associated invasive carcinoma | Senescence is induced in the early stage of intraductal papillary mucinous neoplasm and gradually attenuated according to the progression | [43] |
Cervical and endometrial carcinoma | 77 | Tissues of invasive cervical cancer and endometrial cancer | Squamous cell carcinoma (negative reaction) and cylindrocellular carcinoma (positive reaction in cancer cells) | [44] |
Usual type uterine leiomyoma | 14 (86 samples) |
Fibroid tissue sections | 48 out of 82 tumors were SA-β-gal positive in >10% of the tumor volume. The more senescent cells, the higher the stage (1–4) and the lower the growth potential of the tumor |
[45] |