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. 2021 Nov 22;9:86. doi: 10.1186/s40364-021-00342-4

Table 1.

Nucleases in correlation with cancer types

Name and type of nuclease Type of cancer Nuclease alteration References

FEN1

DNase/RNase, endonuclease, exonuclease

uterine, colon, lung, and kidney cancer Over expression of mRNA [24]
breast, gastric Overexpression of mRNA and protein [24, 25]

APE1

DNase, endonuclease

non–small cell lung-cancer High expression at protein level, difference in subcellular expression patterns between cancer and benign [26, 27]
lung cancer lower enzymatic activity correlated with higher risk [20]
ovarian staining limited to the nuclei in healthy tissues, both nuclear and cytoplasmic expression was detected in cancer tissues [28]
gastric

Nuclear staining more prevalent than cytoplasmic staining in cancer tissues

Elevated serum protein associated with lymph node metastasis

[29, 30]
gastro-esophageal overexpression [29]
breast

overexpression

Increased cancer susceptibility correlated with the SNP variant Asp148Glu

[29, 31, 32]
pancreatico-biliary Overexpression, negative cytoplasmic expression with nuclear APE1 expression correlated with poor tumor differentiation, greater stage and vascular invasion [29]
prostate cancer and prostatic intraepithelial neoplasia Increased cytoplasmic and nuclear expression [33]
human hepatocellular carcinoma upregulation, elevated serum levels [34, 35]
bladder Elevated serum concentration [36]
colorectal

stem cells exhibit higher expression compared with non-stem cells

Asp148Glu and hOGG1 Ser326Cys polymorphisms associated with increased risk, higher frequency of the polymorphisms detected in blood samples from CRC patients compared with healthy subjects

[37, 38]
head and neck correlation between loss of nuclear expression and better prognosis and treatment response [39]
melanoma high expression at mRNA level correlated with poor survival [40]

XPF/XPG

DNase, endonuclease

Lung, cervical and ovarian

ERCC1 overexpression associated with poor response to platinum-based chemotherapy

Poor overall survival in ovarian cancer associated with high expression of XPG at RNA level

[21, 41]
non-small cell lung cancer Improved treatment response correlated with negative staining of tumor sample [42]
melanoma ERCC1 deficiency correlated with improved response to cisplatin therapy [43]
gastric

improved treatment response and survival in correlation with elevated ERCC1 protein

elevated expression of XPG

[21, 44]
colorectal improved survival in correlation with low ERCC1-mRNA expression in the tumors [45]
osteosarcoma improved treatment response to a platinum-based therapy in XPF and XPG knocked down cell line [46]

MRN Complex

DNase, endonuclease/exonuclease

breast loss of expression in breast cancer tissues [47]
Colorectal mutations in MRE11 resulting in reduced expression of MRE11 and impaired function of the MRN complex [48]
endometrial loss of MRE11 expression, loss of MRE11 correlated with the loss of the other components of the complex, mutations in MRE11 resulting in reduced expression of MRE11 and impaired function of MRN complex [48, 49]
bladder High expression of MRE11 correlated with improved survival [50]
gastric carcinoma with high level microsatellite instability mutations of the intronic poly(T)11 repeat in MRE11 [51]

TREX2

DNase, exonuclease

skin carcinogenesis Knock out mouse model [52]
SCC deregulated expression
HNSCC deregulated expression, decreased relative dsDNase activity in the R156L variant

SND1

RNase, endonuclease

human hepatocellular carcinoma overexpression increased angiogenesis [53, 54]
breast cancer mRNA overexpression correlated with reduced survival [55]
prostate cancer overexpression of protein and mRNA, positive correlation with tumor grade [56]
colon cancer Overexpression of mRNA [57]

DNaseI

endonuclease

gastric carcinoma, colorectal carcinoma high frequency of DNaseI phenotype2 [58, 59]

RNaseL

endonuclease

prostate cancer RNaseL mutations, SNPs [60, 61]
decreased enzymatic activity of the variant [62]
uterine cervix, HNSCC and breast cancer a correlation between increased cancer risk and RNaseL SNP rs3738579 [63]

RNaseI

endonuclease

Pancreatic adenocarcinoma difference in glycosylation between healthy and cancer [64, 65]
Serum RNase activity pancreatic carcinoma elevated serum ribonuclease activity [66]

Table 1 summarizes literature findings about nucleases involved in cancer and alteration of nucleases in correlation with respective cancer types