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A potential target for the prevention and therapy of colon cancer: focused on men's clinical features

  • Yeonhee Pyo1
  • Ki Han Kwon2,*,

1Department of Beauty Cosmetics, College of Biomedical and Health Science, Konkuk University, 27478 Chungju, Republic of Korea

2College of General Education, Kookmin University, 02707 Seoul, Republic of Korea

DOI: 10.22514/jomh.2024.180 Vol.20,Issue 11,November 2024 pp.1-8

Submitted: 04 February 2024 Accepted: 30 May 2024

Published: 30 November 2024

*Corresponding Author(s): Ki Han Kwon E-mail: kihan.kwon@kookmin.ac.kr

Abstract

Colon cancer (CCa) is a prevalent malignancy among men and ranks among the leading causes of cancer-related deaths globally, highlighting the critical need for the development of natural therapeutics for both its treatment and prevention. In this regard, the pharmacological properties of medicinal plants have been extensively studied, revealing their potential in exhibiting anti-cancer, anti-oxidant, anti-mutagenic, anti-inflammatory and anti-angiogenic activities relevant to colon cancer prevention and therapy. Current pharmacologic strategies for colorectal cancer (CRC) treatment are under active investigation, yet a universally accepted gold standard remains elusive. The identification of cancer stem cell (CSC) markers plays a pivotal role in enhancing cancer treatment strategies. It enables the customization of therapeutic approaches and is closely linked with the treatment outcomes and prognosis in CCa patients, particularly concerning cell resistance. 5-Fluorouracil (5-FU), a key component in chemotherapy regimens for CRC, is known for its severe side effects and the potential for developing chemoresistance. Research has shown that Portulaca oleracea extract can inhibit the proliferation of HT29 cancer stem cells at concentrations ranging from 0.07 to 2.25 µg/mL, enhancing the sensitivity of these cells to 5-FU. Moreover, the extract may regulate the growth of CCa stem cells by suppressing the expression of Notch1 and β-catenin genes, thereby interfering with the Notch signaling pathway. This review summarizes the findings of clinical trials involving medicinal plants with promising effects against CRC in men. Given the pharmacological efficacy of these plants, their extracts hold promise as viable alternative treatments for CCa.


Keywords

Colon cancer; Anti-cancer; Anti-oxidant; Anti-inflammatory; Pharmacological plants


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Yeonhee Pyo,Ki Han Kwon. A potential target for the prevention and therapy of colon cancer: focused on men's clinical features. Journal of Men's Health. 2024. 20(11);1-8.

References

[1] Esmeeta A, Adhikary S, Dharshnaa V, Swarnamughi P, Ummul Maqsummiya Z, Banerjee A, et al. Plant-derived bioactive compounds in colon cancer treatment: an updated review. Biomedicine & Pharmacotherapy. 2022; 153: 113384.

[2] Yaghoubi A, Khazaei M, Avan A, Hasanian SM, Soleimanpour S. The bacterial instrument as a promising therapy for colon cancer. International Journal of Colorectal Disease. 2020; 35: 595–606.

[3] Fabregas JC, Ramnaraign B, George TJ. Clinical updates for colon cancer care in 2022. Clinical Colorectal Cancer. 2022; 21: 198–203.

[4] Nelson VK, Sahoo NK, Sahu M, Sudhan HH, Pullaiah CP, Muralikrishna KS. In vitro anticancer activity of Eclipta alba whole plant extract on colon cancer cell HCT-116. BMC Complementary Medicine and Therapies. 2020; 20: 355.

[5] Islam MR, Akash S, Rahman MM, Nowrin FT, Akter T, Shohag S, et al. Colon cancer and colorectal cancer: prevention and treatment by potential natural products. Chemico-Biological Interactions. 2022; 368: 110170.

[6] Revathi S, Hakkim FL, Ramesh Kumar N, Bakshi HA, Sangilimuthu AY, Tambuwala MM, et al. In vivo anti cancer potential of pyrogallol in murine model of colon cancer. Asian Pacific Journal of Cancer Prevention. 2019; 20: 2645–2651.

[7] Labianca R, Beretta GD, Kildani B, Milesi L, Merlin F, Mosconi S, et al. Colon cancer. Critical Reviews in Oncology/Hematology. 2010; 74: 106–133.

[8] Mansour-Ghanaei F, Varshi G, Joukar F, Ashoobi MT, Esmaeilpour J, Gharibpoor A, et al. Prevalence of pre-cancerous colon lesions in referred patients under patronage of a local relief foundation in Guilan province. JML Journal of Medicine and Life. 2019; 12: 133–139.

[9] Giovannucci E. Modifiable risk factors for colon cancer. Gastroenterology Clinics of North America. 2002; 31: 925–943.

[10] Roderburg C, Loosen SH, Hoyer L, Luedde T, Kostev K. Prevalence of diabetes mellitus among 80,193 gastrointestinal cancer patients in five European and three Asian countries. Journal of Cancer Research and Clinical Oncology. 2022; 148: 1057–1062.

[11] Gatta G, Capocaccia R, Berrino F, Ruzza MR, Contiero P. Colon cancer prevalence and estimation of differing care needs of colon cancer patients. Annals of Oncology. 2004; 15: 1136–1142.

[12] Gupta R, Bhatt LK, Johnston TP, Prabhavalkar KS. Colon cancer stem cells: Potential target for the treatment of colorectal cancer. Cancer Biology & Therapy. 2019; 20: 1068–1082.

[13] Hines RB, Bimali M, Johnson AM, Bayakly AR, Collins TC. Prevalence and survival benefit of adjuvant chemotherapy in stage III colon cancer patients: comparison of overall and age-stratified results by multivariable modeling and propensity score methodology in a population-based cohort. Cancer Epidemiology. 2016; 44: 77–83.

[14] Kostev K, Krieg S, Krieg A, Luedde T, Loosen SH, Roderburg C. In-hospital mortality and associated factors among colorectal cancer patients in Germany. Cancers. 2024; 16: 1219.

[15] Olde Bekkink M, McCowan C, Falk GA, Teljeur C, Van de Laar FA, Fahey T. Diagnostic accuracy systematic review of rectal bleeding in combination with other symptoms, signs and tests in relation to colorectal cancer. British Journal of Cancer. 2010; 102: 48–58.

[16] Holtedahl K, Borgquist L, Donker GA, Buntinx F, Weller D, Campbell C, et al. Symptoms and signs of colorectal cancer, with differences between proximal and distal colon cancer: a prospective cohort study of diagnostic accuracy in primary care. BMC Primary Care. 2021; 22: 148.

[17] Astin M, Griffin T, Neal RD, Rose P, Hamilton W. The diagnostic value of symptoms for colorectal cancer in primary care: a systematic review. British Journal of General Practice. 2011; 61: e231–e243.

[18] Bousis D, Verras GI, Bouchagier K, Antzoulas A, Panagiotopoulos I, Katinioti A, et al. The role of deep learning in diagnosing colorectal cancer. Przeglad Gastroenterologiczny. 2023; 18: 266–273.

[19] Mulita F, Tepetes K, Verras GI, Liolis E, Tchabashvili L, Kaplanis C, et al. Perineal colostomy: advantages and disadvantages. Przeglad Gastroenterologiczny. 2022; 17: 89–95.

[20] Beniwal SS, Lamo P, Kaushik A, Lorenzo-Villegas DL, Liu Y, MohanaSundaram A. Current status and emerging trends in colorectal cancer screening and diagnostics. Biosensors. 2023; 13: 926.

[21] Pacal I, Karaboga D, Basturk A, Akay B, Nalbantoglu U. A comprehensive review of deep learning in colon cancer. Computers in Biology and Medicine. 2020; 126: 104003.

[22] Yu C, Helwig EJ. The role of AI technology in prediction, diagnosis and treatment of colorectal cancer. Artificial Intelligence Review. 2022; 55: 323–343.

[23] Hann A, Troya J, Fitting D. Current status and limitations of artificial intelligence in colonoscopy. United European Gastroenterology Journal. 2021; 9: 527–533.

[24] Luna JI, Grossenbacher SK, Murphy WJ, Canter RJ. Targeting cancer stem cells with natural killer cell immunotherapy. Expert Opinion on Biological Therapy. 2017; 17: 313–324.

[25] Ruan H, Leibowitz BJ, Zhang L, Yu J. Immunogenic cell death in colon cancer prevention and therapy. Molecular Carcinogenesis. 2020; 59: 783–793.

[26] Garza Treviño EN, Quiroz Reyes AG, Rojas Murillo JA, de la Garza Kalife DA, Delgado Gonzalez P, Islas JF, et al. Cell therapy as target therapy against colon cancer stem cells. International Journal of Molecular Sciences. 2023; 24: 8163.

[27] Sanders MA, Majumdar AP. Colon cancer stem cells: implications in carcinogenesis. Frontiers in Bioscience. 2011; 16: 1651–1662.

[28] Kozovska Z, Gabrisova V, Kucerova L. Colon cancer: cancer stem cells markers, drug resistance and treatment. Biomedicine & Pharmacotherapy. 2014; 68: 911–916.

[29] Wen J, Min X, Shen M, Hua Q, Han Y, Zhao L, et al. ACLY facilitates colon cancer cell metastasis by CTNNB1. Journal of Experimental & Clinical Cancer Research. 2019; 38: 401.

[30] Gerovska D, García-Gallastegi P, Descarpentrie J, Crende O, Casado-Andrés M, Martín A, et al. Proprotein convertases blockage up-regulates specifically metallothioneins coding genes in human colon cancer stem cells. Biochimica et Biophysica Acta-Molecular Cell Research. 2021; 1868: 118912.

[31] Denise C, Paoli P, Calvani M, Taddei ML, Giannoni E, Kopetz S, et al. 5-fluorouracil resistant colon cancer cells are addicted to OXPHOS to survive and enhance stem-like traits. Oncotarget. 2015; 6: 41706–41721.

[32] Mahbub AA. 17β-estradiol enhances 5-fluorouracil anti-cancer activities in colon cancer cell lines. Medical Sciences. 2022; 10: 62.

[33] Liu N, Li J, Zhao Z, Han J, Jiang T, Chen Y, et al. MicroRNA-302a enhances 5-fluorouracil-induced cell death in human colon cancer cells. Oncology Reports. 2017; 37: 631–639.

[34] Hartwig MFS, Gögenur I. Colon cancer surgery in the high-risk patient. Journal of the Danish Medical Association. 2020; 182: V10190572. (In Danish)

[35] Ramshaw BJ. Laparoscopic surgery for cancer patients. CA: A Cancer Journal for Clinicians. 1997; 47: 327–350.

[36] Rossi H, Rothenberger DA. Surgical treatment of colon cancer. Surgical Oncology Clinics of North America. 2006; 15: 109–127.

[37] Zouari A, Masmoudi A, Khanfir F, Ketata S, Rejab H, Bouzid A, et al. Predictive factors for anastomotic leakage after colon cancer surgery. The Pan African Medical Journal. 2022; 42: 129. (In French)

[38] der Hagopian O, Dahlberg M, Heinius G, Nordberg J, Gustafsson J, Nordenvall C, et al. Perirenal fat surface area as a risk factor for perioperative difficulties and 30-day postoperative complications in elective colon cancer surgery. Colorectal Disease. 2018; 20: 1078–1087.

[39] Seo YJ, Kim KE, Jeong WK, Baek SK, Bae SU. Effect of preoperative pan-immune-inflammation value on clinical and oncologic outcomes after colorectal cancer surgery: a retrospective study. Annals of Surgical Treatment and Research. 2024; 106: 169–177.

[40] Koike T, Mukai M, Kishima K, Yokoyama D, Uda S, Hasegawa S, et al. The association between surgical site infection and postoperative colorectal cancer recurrence and the effect of laparoscopic surgery on prognosis. Langenbeck’s Archives of Surgery. 2024; 409: 40.

[41] Hatharaliyadda B, Schmitz M, Mork A, Osman F, Heise C, Safdar N, et al. Surgical site infection prevention using “strike teams”: the experience of an academic colorectal surgical department. Journal for Healthcare Quality. 2024; 46: 22–30.

[42] Esmeeta A, Adhikary S, Dharshnaa V, Swarnamughi P, Ummul Maqsummiya Z, Banerjee A, et al. Plant-derived bioactive compounds in colon cancer treatment: an updated review. Biomedicine & Pharmacotherapy. 2022; 153: 113384.

[43] Prakash MD, Stojanovska L, Feehan J, Nurgali K, Donald EL, Plebanski M, et al. Anti-cancer effects of polyphenol-rich sugarcane extract. PLOS ONE. 2021; 16: e0247492.

[44] Keyvani-Ghamsari S, Rahimi M, Khorsandi K. An update on the potential mechanism of gallic acid as an antibacterial and anticancer agent. Food Science & Nutrition. 2023; 11: 5856–5872.

[45] Rowland I, Gibson G, Heinken A, Scott K, Swann J, Thiele I, Tuohy K. Gut microbiota functions: metabolism of nutrients and other food components. European Journal of Nutrition. 2018; 57: 1–24.

[46] Bié J, Sepodes B, Fernandes PCB, Ribeiro MHL. Polyphenols in health and disease: gut microbiota, bioaccessibility, and bioavailability. Compounds. 2023; 3: 40–72.

[47] Duda-Chodak A, Tarko T. Possible side effects of polyphenols and their interactions with medicines. Molecules. 2023; 28: 2536.

[48] Oliphant K, Allen-Vercoe E. Macronutrient metabolism by the human gut microbiome: major fermentation by-products and their impact on host health. Microbiome. 2019; 7: 91.

[49] Chang L, Liu T, Chai Z, Jie S, Li Z, Liu M, et al. lincRNA-p21 mediates the anti-cancer effect of ginkgo biloba extract EGb 761 by stabilizing E-Cadherin protein in colon cancer. Medical Science Monitor. 2018; 24: 9488–9496.

[50] Zheng YM, Shen JZ, Wang Y, Lu AX, Ho WS. Anti-oxidant and anti-cancer activities of Angelica dahurica extract via induction of apoptosis in colon cancer cells. Phytomedicine. 2016; 23: 1267–1274.

[51] Macharia JM, Mwangi RW, Rozmann N, Zsolt K, Varjas T, Uchechukwu PO, et al. Medicinal plants with anti-colorectal cancer bioactive compounds: potential game-changers in colorectal cancer management. Biomedicine & Pharmacotherapy. 2022; 153: 113383.

[52] Ginovyan M, Babayan A, Shirvanyan A, Minasyan A, Qocharyan M, Kusznierewicz B, et al. The action mechanisms, anti-cancer and antibiotic-modulation potential of Vaccinium myrtillus L. extract. Discovery Medicine. 2023; 35: 590–611.

[53] Koyuncu I, Gönel A, Akdağ A, Yilmaz MA. Identification of phenolic compounds, antioxidant activity and anti-cancer effects of the extract obtained from the shoots of Ornithogalum narbonense L. Cellular and Molecular Biology. 2018; 64: 75–83.

[54] Kuo TT, Lin LC, Chang HY, Chiang PJ, Wu HY, Chen TY, et al. Quantitative proteome analysis reveals melissa officinalis extract targets mitochondrial respiration in colon cancer cells. Molecules. 2022; 27: 4533.

[55] Fahmy MA, Farghaly AA, Hassan EE, Hassan EM, Hassan ZM, Mahmoud K, et al. Evaluation of the anti-cancer/anti-mutagenic efficiency of Lavandula officinalis essential oil. Asian Pacific Journal of Cancer Prevention. 2022; 23: 1215–1222.

[56] Kang HG, Jeong SH, Cho JH. Antimutagenic and anticarcinogenic effect of methanol extracts of Petasites japonicus Maxim leaves. Journal of Veterinary Science. 2010; 11: 51–58.

[57] Yu TW, Xu M, Dashwood RH. Antimutagenic activity of spearmint. Environmental and Molecular Mutagenesis. 2004; 44: 387–393.

[58] Garcia-Lazaro RS, Lamdan H, Caligiuri LG, Lorenzo N, Berengeno AL, Ortega HH, et al. In vitro and in vivo antitumor activity of Yerba Mate extract in colon cancer models. Journal of Food Science. 2020; 85: 2186–2197.

[59] Chiaino E, Micucci M, Durante M, Budriesi R, Gotti R, Marzetti C, et al. Apoptotic-induced effects of Acacia Catechu willd. Extract in human colon cancer cells. International Journal of Molecular Sciences. 2020; 21: 2102.

[60] Jin H, Chen L, Wang S, Chao D. Portulaca oleracea extract can inhibit nodule formation of colon cancer stem cells by regulating gene expression of the Notch signal transduction pathway. Tumor Biology. 2017; 39: 1010428317708699.

[61] Wang W, Li G, Ma J, Fan X, Lu J, Sun Q, et al. Microvascular rarefaction caused by the NOTCH signaling pathway is a key cause of TKI-apatinib-induced hypertension and cardiac damage. Frontiers in Pharmacology. 2024; 15: 1346905.

[62] Kwak M, Southard KM, Kim WR, Lin A, Kim NH, Gopalappa R, et al. Adherens junctions organize size-selective proteolytic hotspots critical for Notch signalling. Nature Cell Biology. 2022; 24: 1739–1753.

[63] Takahashi H, Sakakibara-Konishi J, Furuta M, Shoji T, Tsuji K, Morinaga D, et al. Notch pathway regulates osimertinib drug-tolerant persistence in EGFR-mutated non-small-cell lung cancer. Cancer Science. 2023; 114: 1635–1650.

[64] Johnson SE, Barrick D. Dissecting and circumventing the requirement for RAM in CSL-dependent Notch signaling. PLOS ONE. 2012; 7: e39093.

[65] Lewtak K, Fiołka MJ, Czaplewska P, Macur K, Kaczyński Z, Buchwald T, et al. Sida hermaphrodita seeds as the source of anti-Candida albicans activity. Scientific Reports. 2019; 9: 12233.

[66] Negri M, Salci TP, Shinobu-Mesquita CS, Capoci IR, Svidzinski TI, Kioshima ES. Early state research on antifungal natural products. Molecules. 2014; 19: 2925–2956.

[67] Baba H, Onanuga A. Preliminary phytochemical screening and antimicrobial evaluation of three medicinal plants used in Nigeria. African Journal of Traditional, Complementary and Alternative Medicines. 2011; 8: 387–390.

[68] Singh P, Singh VK, Singh AK. Molecular docking analysis of candidate compounds derived from medicinal plants with type 2 diabetes mellitus targets. Bioinformation. 2019; 15: 179–188.

[69] Sharma H, Yunus GY, Agrawal R, Kalra M, Verma S, Bhattar S. Antifungal efficacy of three medicinal plants Glycyrrhiza glabra, Ficus religiosa, and Plantago major against oral Candida albicans: a comparative analysis. Indian Journal of Dental Research. 2016; 27: 433–436.

[70] Kim J, Jho KH, Choi YH, Nam SY. Chemopreventive effect of cactus (Opuntia humifusa) extracts: radical scavenging activity, pro-apoptosis, and anti-inflammatory effect in human colon (SW480) and breast cancer (MCF7) cells. Food & Function Journal. 2013; 4: 681–688.

[71] Kheyar N, Bellik Y, Serra AT, Kheyar F, Bedjou F. Inula viscosa phenolic extract suppresses colon cancer cell proliferation and ulcerative colitis by modulating oxidative stress biomarkers. BioTechnologia. 2022; 103: 269–281.


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