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. 2018 Sep 25:17:5.
doi: 10.4103/jcar.JCar_7_18. eCollection 2018.

Role of aberrant glycosylation enzymes in oral cancer progression

Affiliations

Role of aberrant glycosylation enzymes in oral cancer progression

Bhairavi N Vajaria et al. J Carcinog. .

Abstract

Background: Carcinogenesis, a multistep process involves sequential changes during neoplastic transformation. The various hallmarks of cancer aid in cell survival, proliferation, and dissemination. Aberrant glycosylation, a recently defined hallmark of cancer, is influenced by glycosylation enzymes during carcinogenesis. Therefore, the present study measured α-2,3 and α-2,6 sialyltransferase (ST), sialidase, and α-L-fucosidase activity in patients with oral precancerous conditions (OPC) and oral cancer patients.

Subjects: The study enrolled 100 oral cancer patients, 50 patients with OPC, 100 healthy controls, and 46 posttreatment follow-ups of oral cancer patients. Blood and saliva were collected from all the participants.

Materials and methods: Sialidase activity was measured by spectrofluorimetric method, α-2,3 and α-2,6 ST by ELISA using biotinylated lectins, and α-L-fucosidase by spectrophotometric method.

Results: The results depicted increased levels of sialidase, α-2,3 and α-2,6 ST, α-L-fucosidase in patients with OPC and oral cancer patients. Receiver operating characteristic curve indicated significant discriminatory efficacy in distinguishing controls and oral cancer patients for serum and salivary sialidase and α-L-fucosidase activity, and serum α-2,6 ST. Furthermore, serum and salivary α-L-fucosidase activity and serum sialidase activity significantly distinguished controls and patients with OPC. Serum and salivary sialidase, α-L-fucosidase, and serum α-2,3 ST activity were higher in patients with metastasis as compared to nonmetastatic patients. Higher values of serum α-L-fucosidase activity were significantly associated with low-overall survival.

Conclusion: The increased levels of enzymes correlated with tumor initiation, progression, and metastasis in oral cancer patients. The alterations in glycosyltransferases/glycosidases thus support the view of glycosylation as a hallmark of cancer.

Keywords: Fucosidase; fucosyltransferase; glycosylation; glycosyltransferase; hallmark; oral cancer; saliva; sialidase; sialyltransferase.

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Conflict of interest statement

There are no conflicts of interest.

Figures

Figure 1
Figure 1
(a) Levels of serum sialidase, α-2,3 and α-2,6 sialyltransferase and α-L-fucosidase enzymes in controls, patients with oral precancerous conditions and oral cancer patients. The values are expressed as mean ± standard error of mean in mU/mg protein. (b) Levels of salivary sialidase, α-2,3 sialyltransferase, α-2,6 sialyltransferase, and α-L-fucosidase enzymes in controls, patients with oral precancerous conditions and oral cancer patients. The values are expressed as Mean ± standard error of mean in mU/mg protein
Figure 2
Figure 2
(a) Serum α-L-fucosidase, α-2,3 and α-2,6 sialyltransferase and sialidase in PT, complete responder and nonresponders patients. The values are expressed as mean ± standard error of mean in mU/mg protein PTc: Pretreatment levels of CR, PTn: Pretreatment levels of nonresponders. (b) Salivary α-L-fucosidase, α-2,3 and α-2,6 sialyltransferase and sialidase in pretreatment, complete responder and nonresponders patients. The values are expressed as mean ± standard error of mean in mu/mg protein PTc: Pretreatment levels of CR, PTn: Pretreatment levels of nonresponders

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References

    1. Hanahan D, Weinberg RA. The hallmarks of cancer. Cell. 2000;100:57–70. - PubMed
    1. Hanahan D, Weinberg RA. Hallmarks of cancer: The next generation. Cell. 2011;144:646–74. - PubMed
    1. Vajaria BN, Patel PS. Glycosylation: A hallmark of cancer? Glycoconj J. 2017;34:147–56. - PubMed
    1. Miyoshi E, Uozumi N, Sobajima T, Takamatsu S, Kamada Y. In: Mechanisms of Malignant Phenotypes. Springer: Japan; 2016. Roles of fucosyltransferases in cancer phenotypes. Glycosignals in cancer; pp. 3–16.
    1. Shah MH, Telang SD, Shah PM, Patel PS. Tissue and serum α2-3-and α2-6-linkage specific sialylation changes in oral carcinogenesis. Glycoconj J. 2008;25:279–90. - PubMed