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What is it?

Shark cartilage is the tissue that provides support for fins in sharks (Squalus acanthias). It mainly comes from sharks caught in the Pacific Ocean.

Shark cartilage became a popular medicine in the 1970s. But its popularity led to a decline in shark numbers. It was previously suggested that sharks don’t get cancer, so consuming their cartilage might help prevent cancer in humans. But it is now clear that sharks do get cancer, and research hasn’t shown benefits for cancer in humans.

People use shark cartilage for cancer, scaly itchy skin (psoriasis), osteoarthritis, and many other conditions, but there is no good scientific evidence supporting these uses.

Don’t confuse shark cartilage with bovine cartilage, or with chondroitin, which can be sourced from shark cartilage.

How effective is it?

Natural Medicines Comprehensive Database rates effectiveness based on scientific evidence according to the following scale: Effective, Likely Effective, Possibly Effective, Possibly Ineffective, Likely Ineffective, Ineffective, and Insufficient Evidence to Rate.

The effectiveness ratings for SHARK CARTILAGE are as follows:

Likely ineffective for…

  • Cancer. Taking shark cartilage by mouth does not benefit people with advanced, previously treated cancers, including breast, colon, lung, prostate, and brain cancer.

There is interest in using shark cartilage for a number of other purposes, but there isn’t enough reliable information to say whether it might be helpful.

Is it safe?

When taken by mouth: Shark cartilage is possibly safe when used for up to 40 months. It can cause a bad taste in the mouth, nausea, vomiting, stomach upset, and constipation.

When applied to the skin: Shark cartilage is possibly safe when used for up to 8 weeks.

Special precautions & warnings:

Pregnancy and breast-feeding: There isn’t enough reliable information to know if shark cartilage is safe to use when pregnant or breast-feeding. Stay on the safe side and avoid use.

“Autoimmune diseases” such as multiple sclerosis (MS), lupus (systemic lupus erythematosus, SLE), rheumatoid arthritis (RA), or other conditions: Shark cartilage might cause the immune system to become more active. This could increase the symptoms of autoimmune diseases. If you have one of these conditions, it’s best to avoid using shark cartilage.

High calcium levels (hypercalcemia): Shark cartilage contains calcium and might increase calcium levels. Do not use shark cartilage if you already have high calcium levels.

Are there interactions with medications?

Moderate
Be cautious with this combination.
Medications that decrease the immune system (Immunosuppressants)
Shark cartilage can increase the activity of the immune system. Some medications, such as those used after a transplant, decrease the activity of the immune system. Taking shark cartilage along with these medications might decrease the effects of these medications.

Are there interactions with herbs and supplements?

Calcium
Shark cartilage contains calcium and might raise calcium levels. Using it along with calcium supplements might make calcium levels too high.

Are there interactions with foods?

Acidic fruit juices such as orange, apple, grape, or tomato, can lower the strength of shark cartilage. If shark cartilage is added to a fruit juice to improve flavor, it should be consumed right away.

How is it typically used?

There isn’t enough reliable information to know what an appropriate dose of shark cartilage might be. Keep in mind that natural products are not always necessarily safe and dosages can be important. Be sure to follow relevant directions on product labels and consult a healthcare professional before using.

Other names

AE-941, Cartilage de Requin, Cartilage de Requin du Pacifique, Cartilago de Tiburon, Collagène Marin, Extrait de Cartilage de Requin, Liquide de Cartilage Marin, Marine Collagen, Marine Liquid Cartilage, MSI-1256F, Neovastat, Pacific Shark Cartilage, Poudre de Cartilage de Requin, Shark Cartilage Powder, Shark Cartilage Extract, Sphyrna lewini, Squalus acanthias.

Methodology

To learn more about how this article was written, please see the Natural Medicines Comprehensive Database methodology.

References

  1. Merly L, Smith SL. Pro-inflammatory properties of shark cartilage supplement. Immunopharmacol Immunotoxicol. 2015;37:140-7. View abstract.
  2. Sakai S, Otake E, Toida T, Goda Y. Identification of the origin of chondroitin sulfate in “health foods”. Chem Pharm Bull (Tokyo). 2007;55:299-303. View abstract.
  3. PDQ Integrative, Alternative, and Complementary Therapies Editorial Board. Cartilage (Bovine and Shark) (PDQ®): Health Professional Version. PDQ Cancer Information Summaries [Internet]. Bethesda (MD): National Cancer Institute (US); 2002. 2016 Jul 21. View abstract.
  4. Goldman E. Shark cartilage extract tried as a novel psoriasis treatment. Skin All News 1998;29:14.
  5. Food and Drug Administration. FDA takes action against firm marketing unapproved drugs. FDA talk paper (December 10, 1999)
  6. Lane W and Milner M. A comparison of shark cartilage and bovine cartilage. Townsend Lett 1996;153:40-42.
  7. Zhuang, L, Wang, B, Shivji, G, and et al. AE-941, a novel inhibitor of angiogenesis has significant anti-inflammatory effect on contact hypersensitivity. J Invest Derm 1997;108:633.
  8. Turcotte P. Phase I dose escalation study of AE-941, an antiangiogenic agent, in age-related macular degeneration patient. Retina Society Conference (Hawaii, December 2, 1999).
  9. Saunder DN. Angiogenesis antagonist as treatment for psoriasis: Phase I clinical trial results with AE-941. American Academy of Dermatology Conference, New Orleans, Louisiana, March 19-24, 1999.
  10. Aeterna Laboratories Inc. Phase III randomized study of AE-941 (Neovastat; Shark Cartilage Extract) in patients with metastatic renal cell carcinoma refractory to immunotherapy. 2001.
  11. Escudier, B, Patenaude, F, Bukowski, R, and et al. Rationale for a phase III clinical trial with AE-941 (Neovastat (R)) in metastatic renal cell carcinoma patients refractory to immunotherapy. Ann Oncol 2000;11(supplement 4):143-144.
  12. Dupont E, Alaoui-Jamali M, Wang T, and et al. Angiostatic and antitumoral activity of AE-941 (Neovastat), a molecular fraction derived from shark cartilage. Proceedings of the American Association for Cancer Research 1997;38:227.
  13. Shimizu-Suganuma, Masum, Mwanatambwe, Milanga, Iida, Kazum, and et al. Effect of shark cartilage on tumor growth and survival time in vivo (meeting abstract). Proc Annu Meet Am Soc Clin Oncol 1999;18:A1760.
  14. Anonymous. Angiostatic and antitumoral activity of AE-941 (neovastat-R), a molecular fraction derived from shark cartilage (meeting abstract). Proc Annu Meet Am Assoc Cancer Res 1997;38:A1530.
  15. Cataldi, JM and Osborne, DL. Effects of shark cartilage on mammary tumor neovascularization in vivo and cell proliferation in vitro (meeting abstract). FASEB Journal 1995;9:A135.
  16. Jamali MA, Riviere P, Falardeau A, and et al. Effect of AE-941 (Neovastat), an angiogenesis inhibitor, in the Lewis lung carcinoma metastatic model, efficacy, toxicity prevention and survival. Clin Invest Med 1998;(suppl):S16.
  17. Saad F, Klotz L, Babaian R, Lacombe L, Champagne P, and Dupont E. Phase I/II trial on AE-941 (Neovastat) in patients with metastatic refractory prostate cancer (abstract presentation). Canadian Urological Association Annual Meeting (June 24-27, 2001).
  18. Rosenbluth, RJ, Jennis, AA, Cantwell, S, and et al. Oral shark cartilage in the treatment of patients with advanced primary brain tumors. A phase II pilot study (meeting abstract). Proc Annu Meet Am Soc Clin Oncol 1999;18:A554.
  19. Dupont E, Savard RE, Jourdain C, Juneau C, Thibodeau A, Ross N, and et al. Antiangiogenic properties of a novel shark cartilage extract: potential role in the treatment of psoriasis. J Cutan Med Surg 1998;2:146-152.
  20. Lane IW and Contreras E. High rate of bioactivity (reduction in gross tumor size) observed in advanced cancer patients treated with shark cartilage material. J Naturopath Med 1992;3:86-88.
  21. Wilson JL. Topical shark cartilage subdues psoriasis. Altern Comp Ther 2000;6:291.
  22. Riviere M, Latreille J, and Falardeau P. AE-941 (Neovastat), an inhibitor of angiogenesis: phase I/II cancer clinical trial results. Cancer Invest 1999;17(suppl 1):16-17.
  23. Milner M. A guide to the use of shark cartilage in the treatment of arthritis and other inflammatory joint diseases. Amer Chiropractor 1999;21:40-42.
  24. Leitner SP, Rothkopf MM, Haverstick DD, and et al. Two phase II studies of oral dry shark cartilage powder (SCP) in patients with either metastatic breast or prostate cancer refractory to standard treatment. Amer Soc Clin Oncol 1998;17:A240.
  25. Evans WK, Latreille J, Batist G, and et al. AE-941, an inhibitor of angiogenesis: rationale for development in combination with induction chemotherapy/radiotherapy in patients with non-small-cell lung cancer (NSCLC). Proffered Papers 1999;S250.
  26. Riviere M, Falardeau P, Latreille J, and et al. Phase I/II lung cancer clinical trial results with AE-941 (Neovastat ®) an inhibitor of angiogenesis. Clin Invest Med (supplement) 1998;S14.
  27. Riviere M, Alaoui-Jamali M, Falardeau P, and et al. Neovastat: an inhibitor of angiogenesis with anti-cancer activity. Proc Amer Assoc Cancer Res 1998;39:46.
  28. No authors. Neovastat clinical trial abstracts. 2001;
  29. Aeterna Laboratories Inc. Phase II study of AE-941 (Neovastat; Shark Cartilage) in patients with early relapse or refractory multiple myeloma. 2001. Information Contact Number 1-888-349-3232.
  30. Felzenszwalb, I., Pelielo de Mattos, J. C., Bernardo-Filho, M., and Caldeira-de-Araujo, A. Shark cartilage-containing preparation: protection against reactive oxygen species. Food Chem Toxicol 1998;36:1079-1084. View abstract.
  31. Coppes, M. J., Anderson, R. A., Egeler, R. M., and Wolff, J. E. Alternative therapies for the treatment of childhood cancer. N Engl.J Med 9-17-1998;339:846-847. View abstract.
  32. Davis, P. F., He, Y., Furneaux, R. H., Johnston, P. S., Ruger, B. M., and Slim, G. C. Inhibition of angiogenesis by oral ingestion of powdered shark cartilage in a rat model. Microvasc.Res 1997;54:178-182. View abstract.
  33. McGuire, T. R., Kazakoff, P. W., Hoie, E. B., and Fienhold, M. A. Antiproliferative activity of shark cartilage with and without tumor necrosis factor-alpha in human umbilical vein endothelium. Pharmacotherapy 1996;16:237-244. View abstract.
  34. Kuettner, K. E. and Pauli, B. U. Inhibition of neovascularization by a cartilage factor. Ciba Found.Symp. 1983;100:163-173. View abstract.
  35. Lee, A. and Langer, R. Shark cartilage contains inhibitors of tumor angiogenesis. Science 9-16-1983;221:1185-1187. View abstract.
  36. Korman, D. B. [Antiangiogenic and antitumor properties of cartilage]. Vopr.Onkol. 2012;58:717-726. View abstract.
  37. Patra, D. and Sandell, L. J. Antiangiogenic and anticancer molecules in cartilage. Expert.Rev Mol.Med 2012;14:e10. View abstract.
  38. de Mejia, E. G. and Dia, V. P. The role of nutraceutical proteins and peptides in apoptosis, angiogenesis, and metastasis of cancer cells. Cancer Metastasis Rev 2010;29:511-528. View abstract.
  39. Bargahi, A., Hassan, Z. M., Rabbani, A., Langroudi, L., Noori, S. H., and Safari, E. Effect of shark cartilage derived protein on the NK cells activity. Immunopharmacol.Immunotoxicol. 2011;33:403-409. View abstract.
  40. Lee, S. Y. and Chung, S. M. Neovastat (AE-941) inhibits the airway inflammation via VEGF and HIF-2 alpha suppression. Vascul.Pharmacol 2007;47(5-6):313-318. View abstract.
  41. Porter, M. E., Koob, T. J., and Summers, A. P. The contribution of mineral to the material properties of vertebral cartilage from the smooth-hound shark Mustelus californicus. J Exp Biol 2007;210(Pt 19):3319-3327. View abstract.
  42. Pearson, W., Orth, M. W., Karrow, N. A., Maclusky, N. J., and Lindinger, M. I. Anti-inflammatory and chondroprotective effects of nutraceuticals from Sasha’s Blend in a cartilage explant model of inflammation. Mol Nutr Food Res 2007;51:1020-1030. View abstract.
  43. Kim, S., de, A., V, Bouajila, J., Dias, A. G., Cyrino, F. Z., Bouskela, E., Costa, P. R., and Nepveu, F. Alpha-phenyl-N-tert-butyl nitrone (PBN) derivatives: synthesis and protective action against microvascular damages induced by ischemia/reperfusion. Bioorg.Med Chem 5-15-2007;15:3572-3578. View abstract.
  44. Merly, L., Simjee, S., and Smith, S. L. Induction of inflammatory cytokines by cartilage extracts. Int Immunopharmacol. 2007;7:383-391. View abstract.
  45. Moses, M. A., Sudhalter, J., and Langer, R. Identification of an inhibitor of neovascularization from cartilage. Science 6-15-1990;248:1408-1410. View abstract.
  46. Deng, B. and Zhang, Z. [Determination of trace elements in shark cartilage by inductively coupled plasma atomic emission spectrometry]. Guang.Pu.Xue.Yu Guang.Pu.Fen.Xi. 1998;18:570-575. View abstract.
  47. Ratel, D., Glazier, G., Provencal, M., Boivin, D., Beaulieu, E., Gingras, D., and Beliveau, R. Direct-acting fibrinolytic enzymes in shark cartilage extract: potential therapeutic role in vascular disorders. Thromb.Res. 2005;115(1-2):143-152. View abstract.
  48. Gingras, D., Labelle, D., Nyalendo, C., Boivin, D., Demeule, M., Barthomeuf, C., and Beliveau, R. The antiangiogenic agent Neovastat (AE-941) stimulates tissue plasminogen activator activity. Invest New Drugs 2004;22:17-26. View abstract.
  49. Latreille, J., Batist, G., Laberge, F., Champagne, P., Croteau, D., Falardeau, P., Levinton, C., Hariton, C., Evans, W. K., and Dupont, E. Phase I/II trial of the safety and efficacy of AE-941 (Neovastat) in the treatment of non-small-cell lung cancer. Clin Lung Cancer 2003;4:231-236. View abstract.
  50. Bukowski, R. M. AE-941, a multifunctional antiangiogenic compound: trials in renal cell carcinoma. Expert.Opin.Investig.Drugs 2003;12:1403-1411. View abstract.
  51. Jagannath, S., Champagne, P., Hariton, C., and Dupont, E. Neovastat in multiple myeloma. Eur.J.Haematol. 2003;70:267-268. View abstract.
  52. FDA grants orphan-drug status to Aeterna’s Neovastat for kidney cancer. Expert.Rev Anticancer Ther 2002;2:618. View abstract.
  53. Dupont, E., Falardeau, P., Mousa, S. A., Dimitriadou, V., Pepin, M. C., Wang, T., and Alaoui-Jamali, M. A. Antiangiogenic and antimetastatic properties of Neovastat (AE-941), an orally active extract derived from cartilage tissue. Clin Exp Metastasis 2002;19:145-153. View abstract.
  54. Beliveau, R., Gingras, D., Kruger, E. A., Lamy, S., Sirois, P., Simard, B., Sirois, M. G., Tranqui, L., Baffert, F., Beaulieu, E., Dimitriadou, V., Pepin, M. C., Courjal, F., Ricard, I., Poyet, P., Falardeau, P., Figg, W. D., and Dupont, E. The Antiangiogenic Agent Neovastat (AE-941) Inhibits Vascular Endothelial Growth Factor-mediated Biological Effects. Clin Cancer Res 2002;8:1242-1250. View abstract.
  55. Weber, M. H., Lee, J., and Orr, F. W. The effect of Neovastat (AE-941) on an experimental metastatic bone tumor model. Int J Oncol 2002;20:299-303.
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