Tumor-associated glycoprotein 72
Tumor-associated glycoprotein 72 (TAG-72) is a glycoprotein that appears on the surface of many cancer cells, including those from the ovary,[1][2][3] breast, colon,[4] lung, and pancreatic cancers.[5][6] TAG-72 is a mucin-like molecule with a molar mass of over 1000 kDa, and is classified as a tumor-associated glycoprotein.[7]
Discovery
Researchers identified Tumor-associated glycoprotein 72 (TAG-72) in the mid-1980s during the development of the Monoclonal antibody B72.3. These antibodies selectively bound to a high-molecular-weight glycoprotein found on various Carcinoma cells. Later studies confirmed TAG-72 as a Mucin-like molecule with significant Glycosylation, which adds to its high molecular weight.[8] This discovery has supported advancements in cancer diagnostics and therapeutics, especially those targeting TAG-72-expressing tumors.[9]
Structure

TAG-72 is a high-molecular-weight glycoprotein(>1,000 Kda), primarily expressed on the surface of various Adenocarcinomas. Its structure is features extensive O-linked glycosylation,[9] which gives it a mucin-like configuration.[9][10][8] The glycosylation patterns of TAG-72 include tumor-associated carbohydrate antigens such assialyl-Tn (STn) and Thomsen–Friedenreich antigens, which are contribute to tumor progression and metastasis.[11] These carbohydrate epitopes serve as binding sites for monoclonal antibodies like B72.3 and CC49, enabling targeted cancer detection and treatment.[9]
Pathogenic mechanism
TAG-72 rarely appears in normal adult tissues but is highly present in malignant epithelial cells, which makes it a Tumor-specific antigen.[8] It plays a role in:
- Tumor Progression: TAG-72 forms part of the mucinous barrier that shields tumor cells from immune recognition.[12]
- Cell Adhesion and Metastasis: Its Glycosylation influences how tumor cells interact with the extracellular matrix, facilitating metastasis.[13]
Clinical applications
1. Tumor Marker (CA 72-4 Assay)

TAG-72 is commonly measured with radioimmunoassays like CA 72-4,[14] which uses the monoclonal antibodies indium (111In) satumomab pendetide and iodine (125I) minretumomab.[15][16][17][18][19] This assay has a good specificity for gastric cancer, with a correlation to the neoplasia's extension. It is used for:
- Cancer diagnosis and staging[20]
- Monitoring recurrence and therapy effectiveness
- Targeted Cancer Therapies[9]
Since TAG-72 is tumor-specific, it is a promising target for immunotherapy and antibody-drug conjugates:
- Monoclonal Antibody Therapy:
- Minretumomab (CC49) has been studied for targeting TAG-72 in solid tumors.[21]
- Anatumomab mafenatox is an anti-TAG-72 antibody conjugated with toxins for cancer treatment.[22]
 
- CAR-T Cell Therapy: CAR-T cells engineered to recognize TAG-72 have been tested in ovarian and colorectal cancer.[23]
Cancer association
TAG-72 is mainly found in epithelial-derived malignancies, including:
Gastrointestinal
- Colorectal cancer: TAG-72 is overexpressed in colorectal Adenocarcinoma, and serum levels often reflect tumor stage and prognosis[24]
- Gastric cancer: CA 72-4, an immunoassay detecting TAG-72, is widely used for diagnosing and monitoring gastric cancer.[25]
- Pancreatic cancer: TAG-72 levels have helped in diagnosing late stage pancreatic cancers.[26]
Gynecological
- Ovarian cancer: TAG-72 expression correlates with tumor stage and patient prognosis.[27]
Other cancers
- Lung cancer: TAG-72 is present in a subset of non-small cell lung carcinomas.[28]
- Breast cancer: Although less specific, TAG-72 has been detected in certain aggressive breast cancer subtypes.[29]
References
- ^ Ponnusamy MP, Venkatraman G, Singh AP, Chauhan SC, Johansson SL, Jain M, et al. (2007-06-28). "Expression of TAG-72 in ovarian cancer and its correlation with tumor stage and patient prognosis". Cancer Letters. 251 (2): 247–257. doi:10.1016/j.canlet.2006.11.025. PMID 17210225.
- ^ Murad JP, Kozlowska AK, Lee HJ, Ramamurthy M, Chang WC, Yazaki P, et al. (2018-11-19). "Effective Targeting of TAG72+ Peritoneal Ovarian Tumors via Regional Delivery of CAR-Engineered T Cells". Frontiers in Immunology. 9: 2268. doi:10.3389/fimmu.2018.02268. PMC 6254427. PMID 30510550.
- ^ Shu R, Evtimov VJ, Hammett MV, Nguyen NN, Zhuang J, Hudson PJ, et al. (2021-01-16). "Engineered CAR-T cells targeting TAG-72 and CD47 in ovarian cancer". Molecular Therapy Oncolytics. 20: 325–341. doi:10.1016/j.omto.2021.01.002. PMC 7868933. PMID 33614914.
- ^ Hege KM, Bergsland EK, Fisher GA, Nemunaitis JJ, Warren RS, McArthur JG, et al. (2017-03-21). "Safety, tumor trafficking and immunogenicity of chimeric antigen receptor (CAR)-T cells specific for TAG-72 in colorectal cancer". Journal for Immunotherapy of Cancer. 5 22. doi:10.1186/s40425-017-0222-9. PMC 5360066. PMID 28344808.
- ^ TAG-72 antigen entry in the public domain NCI Dictionary of Cancer Terms
- ^ Scott AM, Wolchok JD, Old LJ (Mar 2012). "Antibody therapy of cancer". Nature Reviews. Cancer. 12 (4): 278–287. doi:10.1038/nrc3236. PMID 22437872. S2CID 205469234.
- ^ Sheer DG, Schlom J, Cooper HL (Dec 1988). "Purification and Composition of the Human Tumor-associated Glycoprotein (TAG-72) Defined by Monoclonal Antibodies CC49 and B72.3". Cancer Research. 48 (23): 6811–6818. PMID 3180090.
- ^ a b c Chopra A (2004), "99mTc-Labeled tumor-associated glycoprotein 72 binding peptides A2-6 and A3-10", Molecular Imaging and Contrast Agent Database (MICAD), Bethesda (MD): National Center for Biotechnology Information (US), PMID 22049573, retrieved 2025-04-19
- ^ a b c d e f Hitchcock CL, Povoski SP, Mojzisik CM, Martin EJ (2021-12-07). "Survival Advantage Following TAG-72 Antigen-Directed Cancer Surgery in Patients With Colorectal Carcinoma: Proposed Mechanisms of Action". Frontiers in Oncology. 11: 731350. doi:10.3389/fonc.2021.731350. ISSN 2234-943X. PMC 8688248. PMID 34950576.
- ^ Riley NM, Wen RM, Bertozzi CR, Brooks JD, Pitteri SJ (2023). "Measuring the multifaceted roles of mucin-domain glycoproteins in cancer". Advances in Cancer Research. 157: 83–121. doi:10.1016/bs.acr.2022.09.001. ISBN 978-0-323-99177-3. ISSN 2162-5557. PMC 10582998. PMID 36725114.
- ^ Rajesh C, Radhakrishnan P (2023-01-06). "The (Sialyl) Tn antigen: Contributions to immunosuppression in gastrointestinal cancers". Frontiers in Oncology. 12: 1093496. doi:10.3389/fonc.2022.1093496. ISSN 2234-943X. PMC 9852904. PMID 36686742.
- ^ Bhatia R, Gautam SK, Cannon A, Thompson C, Hall BR, Aithal A, et al. (June 2019). "Cancer-associated mucins: role in immune modulation and metastasis". Cancer and Metastasis Reviews. 38 (1–2): 223–236. doi:10.1007/s10555-018-09775-0. ISSN 1573-7233. PMC 6614013. PMID 30618016.
- ^ Laubli H, Borsig L (2019). "Altered Cell Adhesion and Glycosylation Promote Cancer Immune Suppression and Metastasis". Frontiers in Immunology. 10: 2120. doi:10.3389/fimmu.2019.02120. ISSN 1664-3224. PMC 6743365. PMID 31552050.
- ^ Guadagni F, Roselli M, Amato T, Cosimelli M, Perri P, Casale V, et al. (1992-03-01). "CA 72-4 measurement of tumor-associated glycoprotein 72 (TAG-72) as a serum marker in the management of gastric carcinoma". Cancer Research. 52 (5): 1222–1227. ISSN 0008-5472. PMID 1737383.
- ^ Louhimo J, Alfthan H, Stenman UH, Haglund C (2004). "Serum HCG beta and CA 72-4 are stronger prognostic factors than CEA, CA 19-9 and CA 242 in pancreatic cancer". Oncology. 66 (2): 126–131. doi:10.1159/000077438. PMID 15138364. S2CID 25798287.
- ^ Louhimo J, Carpelan-Holmström M, Alfthan H, Stenman UH, Järvinen HJ, Haglund C (October 2002). "Serum HCG beta, CA 72-4 and CEA are independent prognostic factors in colorectal cancer". International Journal of Cancer. 101 (6): 545–548. doi:10.1002/ijc.90009. PMID 12237895.
- ^ Louhimo J, Kokkola A, Alfthan H, Stenman UH, Haglund C (October 2004). "Preoperative hCGbeta and CA 72-4 are prognostic factors in gastric cancer". International Journal of Cancer. 111 (6): 929–933. doi:10.1002/ijc.20321. PMID 15300805. S2CID 24698852.
- ^ Mattar R, Alves de Andrade CR, DiFavero GM, Gama-Rodrigues JJ, Laudanna AA (2002). "Preoperative serum levels of CA 72-4, CEA, CA 19-9, and alpha-fetoprotein in patients with gastric cancer". Revista do Hospital das Clinicas. 57 (3): 89–92. doi:10.1590/s0041-87812002000300001. PMID 12118264.
- ^ Guadagni F, Roselli M, Cosimelli M, Spila A, Cavaliere F, Tedesco M, et al. (November 1996). "Correlation between tumor-associated glycoprotein 72 mucin levels in tumor and serum of colorectal patients as measured by the quantitative CA 72-4 immunoassay". Cancer Research. 56 (22): 5293–5298. PMID 8912871.
- ^ Guadagni F, Roselli M, Ferroni P, Amato T, Colcher D, Greiner JW, et al. (1991). "Clinical evaluation of the new tumor marker TAG-72". Anticancer Research. 11 (4): 1389–1394. ISSN 0250-7005. PMID 1746895.
- ^ "Anti-TAG-72 [Minretumomab (CC49 )]". Absolute Antibody. Retrieved 2025-04-19.
- ^ "Anti-Human TAG-72 Recombinant Antibody(Anatumomab Mafenatox) - KMD Bioscience-Nanobody Discovery Platform, Protein Expression Systems, and CRO Service Supplier". www.kmdbioscience.com. Retrieved 2025-04-19.
- ^ Shu R, Evtimov VJ, Hammett MV, Nguyen NN, Zhuang J, Hudson PJ, et al. (2021-03-26). "Engineered CAR-T cells targeting TAG-72 and CD47 in ovarian cancer". Molecular Therapy Oncolytics. 20: 325–341. doi:10.1016/j.omto.2021.01.002. ISSN 2372-7705. PMC 7868933. PMID 33614914.
- ^ Cho J, Kim KM, Kim HC, Lee WY, Kang WK, Park YS, et al. (January 2019). "The prognostic role of tumor associated glycoprotein 72 (TAG-72) in stage II and III colorectal adenocarcinoma". Pathology, Research and Practice. 215 (1): 171–176. doi:10.1016/j.prp.2018.10.024. ISSN 1618-0631. PMID 30466765.
- ^ Xu Y, Zhang P, Zhang K, Huang C (2021-12-01). "The application of CA72-4 in the diagnosis, prognosis, and treatment of gastric cancer". Biochimica et Biophysica Acta (BBA) - Reviews on Cancer. 1876 (2) 188634. BBA. doi:10.1016/j.bbcan.2021.188634. ISSN 0304-419X. PMID 34656687.
- ^ Pasquali C, Sperti C, D'Andrea AA, Costantino V, Filipponi C, Pedrazzoli S (June 1994). "Clinical value of serum TAG-72 as a tumor marker for pancreatic carcinoma. Comparison with CA 19-9". International Journal of Pancreatology. 15 (3): 171–177. doi:10.1007/BF02924191. ISSN 0169-4197. PMID 7930777.
- ^ Ponnusamy MP, Venkatraman G, Singh AP, Chauhan SC, Johansson SL, Jain M, et al. (2007-06-28). "Expression of TAG-72 in ovarian cancer and its correlation with tumor stage and patient prognosis". Cancer Letters. 251 (2): 247–257. doi:10.1016/j.canlet.2006.11.025. ISSN 0304-3835. PMID 17210225.
- ^ Chen L, Wang Y, Liu X, Dou S, Liu G, Hnatowich DJ, et al. (2008-12-08). "A new TAG-72 cancer marker peptide identified by phage display". Cancer Letters. 272 (1): 122–132. doi:10.1016/j.canlet.2008.07.009. ISSN 1872-7980. PMC 2680929. PMID 18723274.
- ^ Galietta A, Pizzi C, Pettinato G, Limite G, Sgambato A, Lamberti M, et al. (2002). "Differential TAG-72 epitope expression in breast cancer and lymph node metastases: a marker of a more aggressive phenotype". Oncology Reports. 9 (1): 135–140. ISSN 1021-335X. PMID 11748471.
 This article incorporates public domain material from Dictionary of Cancer Terms. U.S. National Cancer Institute.
 This article incorporates public domain material from Dictionary of Cancer Terms. U.S. National Cancer Institute.