Shiitake Mushroom, Lentinan, and Cancer

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It’s equivocal whether shiitake mushroom supplements benefit any patients with cancer.
It’s equivocal whether shiitake mushroom supplements benefit any patients with cancer.

General Information

The edible mushroom Lentinus edodes is known as shiitake in Japan and xianggu in China.1 It originated in East Asia, where it grows on decaying trees and figures prominently in traditional medicine, but it is now widely cultivated around the world. It is one of several mushrooms with frequently reported but unconfirmed anticancer properties and other health benefits.2-5

Researchers have studied the cellular and health effects of shiitake extracts and isolated shiitake-derived beta-glucan polysaccharides, primarily lentinan, mainly in preclinical settings.4-9 Nearly all of the clinical studies conducted have been uncontrolled cohort studies with mixed results.

Potential Hazards

Consumption of raw or inadequately cooked shiitake can cause extensive erythematous rash, an allergic response known as “shiitake dermatitis.”10-12 Symptoms include lines of red skin rash, pruritus, fever, diarrhea, and mucosal ulcers, according to a recent systematic review.11 Merely handling the raw mushroom can cause contact dermatitis.12 Ingestion might also cause eosinophilia and gastrointestinal problems in some patients.13

Animal experiments suggest that consumption of powdered shiitake can cause leukopenia. A study of 7 patients with cancer found that a shiitake-derived nutritional supplement was immunomodulatory, suppressing lymphocytes and monocytes overall but increasing specific lymphocyte subpopulations, such as CD3/CD4 and natural killer cells.8,9

Evidence in Favor

The evidence of beneficial effects for patients with cancer is limited and equivocal.

Preclinical cell-line and animal studies, largely published by researchers in China, suggests that shiitake extracts or polysaccharides like lentinan (1,3 beta-D-glucan) might have cellular-immunity-enhancing, antioxidative, pro-apoptotic, antiproliferative, and P450-enzyme and tumor-cell inhibiting effects.14

Authors of one recent study conducted in China found that a water-extracted shiitake polysaccharide known as SLNT “significantly inhibited proliferation of HT-29 colon cancer cells and suppressed tumor growth in nude mice.”15 A separate study in China suggested that lentinan might synergize with oxaliplatin to inhibit NF-kB, Stat3, and survivin signaling in HepG2 cell lines and H22 tumor-bearing mice.1

“SLNT induced apoptosis by activating Caspace-3 via both intrinsic and extrinsic pathways, which presented as the activation of Caspases-9 and -8, upregulation of cytochrome c and the Bax/Bcl-2 ratio, downregulation of NF-kB, and overproduction of ROS and TNF [tumor necrosis factor]-α in vitro and in vivo,” they reported.15 “These findings suggest that SLNT exerts direct antitumor effects by inducing cell apoptosis via ROS-mediated intrinsic and TNF-α-mediated extrinsic pathways.”

Early clinical research with small patient cohorts, primarily conducted in Japan, suggests that lentinan is safe and is possibly associated with quality of life and survival time for patients with gastric, liver, and pancreatic cancer, but for the most part, these studies have not been confirmed in larger, randomized, controlled clinical trials.16-18

A 2011-published nonrandomized study of 78 patients with unresectable metastatic or recurrent gastric cancer found that patients receiving lentinan plus paclitaxel or cisplatin chemotherapy experienced longer median overall survival (OS) than those receiving chemotherapy alone (median OS: 689 days vs 565 days; P = .0406).19

The same research team reported in 2016 that 3 patients with unresectable gastric cancer and liver metastases who received lentinan once or twice monthly plus chemotherapy with cisplatin and either paclitaxel or trastuzumab experienced objective tumor responses (1 complete response and 2 partial responses) — but because this was a very small, uncontrolled cohort study, it is not possible to determine the causal role of lentinan in these outcomes.20

A 2002 meta-analysis of data pooled from 5 clinical trials representing 650 patients suggested a modest increase in OS among patients with advanced gastric cancer who were treated with lentinan with chemotherapy over patients receiving chemotherapy alone (hazard ratio [HR] for OS, 0.8; 95% CI, 0.68-0.95).16

Evidence Against

A 2002 cohort study conducted at the University of California, Davis School of Medicine found that shiitake extract did not affect prostate-specific antigen (PSA) levels in 62 men with prostate cancer.21

One randomized phase 3 clinical trial conducted in Japan and published in 2016 found that among patients with gastric cancer, those receiving purified lentinan plus chemotherapy had statistically similar but numerically shorter OS times than patients administered chemotherapy alone (median OS: 9.9 vs 13.8 months; P = .21).22

Patients in the lentinan study group also experienced significantly shorter time to treatment failure (2.6 vs 4.3 months; P < .001).22

Conclusions

Despite promising preclinical research, shiitake and shiitake-derived compounds are not linked to improved survival among patients with cancer in large, well-designed clinical trials.

References

  1. Zhang Y, Li Q, Wang J, et al. Polysaccharide from Lentinus edodes combined with oxaliplatin possesses the synergy and attenuation effect in hepatocellular carcinoma. Cancer Lett. 2016;377:117-25. doi: 10.1016/j.canlet.2016.04.037
  2. Jenkin M. Could mushrooms be the cure for cancer? The Guardian website. https://www.theguardian.com/lifeandstyle/2014/mar/02/could-mushrooms-cure-cancer. Published March 2, 2014. Accessed April 2017.
  3. Money NP. Are mushrooms medicinal? Fung Biol. 2016;120:449-53. doi: 10.1016/j.funbio.2016.01.006
  4. Roupas P, Keogh J, Noakes M, Margetts C, Taylor P. The role of edible mushrooms in health: evaluation of the evidence. J Funct Foods. 2012;4:687-709. doi: 10.1016/j.jff.2012.05.003
  5. Xu T, Beelman RB, Lambert JD. The cancer preventive effects of edible mushrooms. Anticancer Agents Med Chem. 2012;12(10):1255-63.
  6. Fang N, Li Q, Yu S, et al. Inhibition of growth and induction of apoptosis in human cancer cell lines by an ethyl acetate fraction from shiitake mushrooms. J Altern Complement Med. 2006;12(2):125-32.
  7. Wang KP, Zhang QL, Liu Y, Wang J, Cheng Y, Zhang Y. Structure and inducing tumor cell apoptosis activity of polysaccharides isolated from Lentinus edodes. J Agr Food Chem. 2013;61(41):9849-58. doi: 10.1021/jf403291w
  8. Del Buono A, Bonucci M, Pugliese S, D'Orta A, Fioranelli M. Polysaccharide from Lentinus edodes for integrative cancer treatment: immunomodulatory effects on lymphocyte population. World Cancer Res J. 2016;3(1):e652.
  9. Grotto D, Bueno DC, Ramos GK, da Costa SR, Spim SR, Gerenutti M. Assessment of the safety of the shiitake culinary-medicinal mushroom, Lentinus edodes (Agaricomycetes), in rats: biochemical, hematological, and antioxidative parameters. In J Med Mushrooms. 2016;18(10):861-70.
  10. Bachmeyer C, Rouff E. Shiitake dermatitis. CMAJ. 2017;189(11):E439. doi: 10.1503/cmaj.160644
  11. Nguyen AH, Gonzaga MI, Lim V, Adler MJ, Mitkov MV, Cappel MA. Clinical features of shiitake dermatitis: a systematic review. Int J Dermatol. 2017 Jan 4. doi: 10.1111/ijd.13433 [Epub ahead of print]
  12. Stephany M, Chung S, Handler M, Handler NS, Handler GA, Schwartz RA. Shiitake mushroom dermatitis: a review. Am J Clin Dermatol. 2016;17(5):485-9. doi: 10.1007/s40257-016-0212-6
  13. Levy AM, Kita H, Phillips SF, et al. Eosinophilia and gastrointestinal symptoms after ingestion of shiitake mushrooms. J Allergy Clin Immunol. 1998;101(5):613-20.
  14. Yu ZH, Yin LH, Qian Y, Yan L. Effect of Lentinus edodes polysaccharide on oxidative stress, immunity activity and oral ulceration of rats stimulated by phenol. Carbohydr Polym. 2009;75:115-8.
  15. Wang JL, Li WY, Huang X, et al. A polysaccharide from Lentinus edodes inhibits human colon cancer cell proliferation and suppresses tumor growth in athymic nude mice. Oncotarget. 2017;8(1):610-23. doi: 10.18632/oncotarget.13481
  16. Oba K, Kobayashi M, Matsui T, Kodera Y, Sakamoto J. Individual patient based meta-analysis of lentinan for unresectable/recurrent gastric cancer. Anticancer Res. 2009;29:2739-45.
  17. Isoda N, Eguchi Y, Nukaya H, et al. Clinical efficacy of superfine dispersed lentinan (beta-1,3-glucan) in patients with hepatocellular carcinoma. Hepatogastroenterology. 2009;56:437-41.
  18. Shimizu K, Watanabe S, Watanabe S, et al. Efficacy of oral administered superfine dispersed lentinan for advanced pancreatic cancer. Hepatogastroenterology. 2009;56:240-4.
  19. Ina K, Furuta R, Kataoka T, et al. Lentinan prolonged survival in patients with gastric cancer receiving S-1-based chemotherapy. World J Clin Oncol. 2011;2(10):339-43. doi: 10.5306/wjco.v2.i10.339
  20. Ina K, Furuta R, Kayukawa S, Kataoka T. Gastric cancer patients with multiple liver metastases were successfully treated with chemo-immunotherapy using lentinan. Gastroenterol. 2016;150(4, Suppl. 1):S866.
  21. deVere White RW, Hackman RM, Soares SE, Beckett LA, Sun B. Effects of a mushroom mycelium extract on the treatment of prostate cancer. Urology. 2002;60(4):640-4.
  22. Yoshino S, Nishikawa K, Morita S, et al. Randomised phase III study of S-1 alone versus S-1 plus lentinan for unresectable or recurrent gastric cancer (JFMC36-0701). Eur J Cancer. 2016;65:164-71. doi: 10.1016/j.ejca.2016.06.012

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