Gene polymorphisms and post-treatment toxicity and treatment response in head and neck squamous cell carcinoma: A scoping review

被引:0
作者
Rajabi-Moghaddam, Mahdieh [1 ]
Abbaszadeh, Hamid [2 ]
机构
[1] Birjand Univ Med Sci, Sch Med, Dept Pathol, Birjand, Iran
[2] Birjand Univ Med Sci, Sch Dent, Dept Oral & Maxillofacial Pathol, Birjand, Iran
关键词
gene polymorphism; head and neck squamous cell carcinoma; single nucleotide polymorphisms; toxicity; treatment outcome; SINGLE NUCLEOTIDE POLYMORPHISMS; CANCER-PATIENTS; ASSOCIATION; SENSITIVITY; CISPLATIN; SUSCEPTIBILITY; XRCC1;
D O I
10.1002/osi2.1161
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Variations in toxicity and treatment response are observed among patients with head and neck squamous cell carcinomas (HNSCCs) despite similar clinicopathologic characteristics that are attributed to gene polymorphisms. This study aimed to review the literatures about the impact of gene polymorphisms on post-treatment toxicity and treatment response in HNSCCs. A systematic search of all original articles about impact of gene polymorphisms on toxicity and response rate in HNSCCs was done till September 2021 using Google Scholar and PubMed databases. Of 15 345 initial searched articles, 25 articles were finally found to be eligible for inclusion in this review. A total of 41 genes and 69 polymorphisms were examined in these studies. Twenty-nine genes with 42 polymorphisms for treatment response and 21 genes with 33 polymorphisms were examined for post-treatment toxicity. Because each of the Asp312Asn ERCC2, lle105Val GSTP1, and Phe31lle AurkA polymorphisms has been associated with significant results in two studies, these polymorphisms are more likely to be associated with a treatment response. In the same way, the R521K EGFR polymorphism is more likely to be associated with a post-treatment toxicity. Because some polymorphisms such as R521K EGFR, *4 or *6 CYP2D6, and rs396991 Fc gamma RIlla have been associated with significant results in one study (without contradictory study), it is likely that they will be associated with a treatment response by further studies. Due to the paucity of studies, definitive conclusions are impossible, so further studies with meta-analysis in the future are recommended.
引用
收藏
页码:151 / 164
页数:14
相关论文
共 26 条
[1]  
Alsbeih Ghazi Atiyeh, 2008, J Egypt Natl Canc Inst, V20, P302
[2]   Polymorphism of FGFR4 in cancer development and sensitivity to cisplatin and radiation in head and neck cancer [J].
Ansell, Anna ;
Farnebo, Lovisa ;
Grenman, Reidar ;
Roberg, Karin ;
Thunell, Lena K. .
ORAL ONCOLOGY, 2009, 45 (01) :23-29
[3]  
Baumann Alexander, 2018, Oncotarget, V9, P12769, DOI 10.18632/oncotarget.24355
[4]   Matrix metalloproteinase 3 polymorphism:: A predictive factor of response to neoadjuvant chemotherapy in head and neck squamous cell carcinoma [J].
Blons, H ;
Gad, S ;
Zinzindohoué, F ;
Manière, I ;
Beauregard, J ;
Tregouet, D ;
Brasnu, D ;
Beaune, P ;
Laccourreye, O ;
Laurent-Puig, P .
CLINICAL CANCER RESEARCH, 2004, 10 (08) :2594-2599
[5]   Cetuximab Resistance in Head and Neck Cancer Is Mediated by EGFR-K521 Polymorphism [J].
Braig, Friederike ;
Kriegs, Malte ;
Voigtlaender, Minna ;
Habel, Beate ;
Grob, Tobias ;
Biskup, Karina ;
Blanchard, Veronique ;
Sack, Markus ;
Thalhammer, Anja ;
Ben Batalla, Isabel ;
Braren, Ingke ;
Laban, Simon ;
Danielczyk, Antje ;
Goletz, Steffen ;
Jakubowicz, Elzbieta ;
Maerkl, Bruno ;
Trepel, Martin ;
Knecht, Rainald ;
Riecken, Kristoffer ;
Fehse, Boris ;
Loges, Sonja ;
Bokemeyer, Carsten ;
Binder, Mascha .
CANCER RESEARCH, 2017, 77 (05) :1188-1199
[6]   Influence of genetic background and oxidative stress response on risk of mandibular osteoradionecrosis after radiotherapy of head and neck cancer [J].
Danielsson, Daniel ;
Brehwens, Karl ;
Halle, Martin ;
Marczyk, Michal ;
Sollazzo, Alice ;
Polanska, Joanna ;
Munck-Wikland, Eva ;
Wojcik, Andrzej ;
Haghdoost, Siamak .
HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK, 2016, 38 (03) :387-393
[7]   Improved survival of patients with human papillomavirus-positive head and neck squamous cell carcinoma in a prospective clinical trial [J].
Fakhry, Carole ;
Westra, William H. ;
Cmelak, Sigui Li Anthony ;
Ridge, John A. ;
Pinto, Harlan ;
Forastiere, Arlene ;
Gillison, Maura L. .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2008, 100 (04) :261-269
[8]   Proteins and single nucleotide polymorphisms involved in apoptosis, growth control, and DNA repair predict cisplatin sensitivity in head and neck cancer cell lines [J].
Farnebo, Lovisa ;
Jedlinski, Adam ;
Ansell, Anna ;
Vainikka, Linda ;
Thunell, Lena K. ;
Grenman, Reidar ;
Johansson, Ann-Charlotte ;
Roberg, Karin .
INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2009, 24 (04) :549-556
[9]   Epidermal growth factor receptor (EGFR) pathway polymorphisms as predictive markers of cetuximab toxicity in locally advanced head and neck squamous cell carcinoma (HNSCC) in a Spanish population [J].
Fernandez-Mateos, J. ;
Seijas-Tamayo, R. ;
Mesia, R. ;
Taberna, M. ;
Pastor Borgonon, M. ;
Perez-Ruiz, E. ;
Klain, J. C. Adansa ;
Vazquez Fernandez, S. ;
del Barco Morillo, E. ;
Lozano, A. ;
Gonzalez Sarmiento, R. ;
Cruz-Hernandez, J. J. .
ORAL ONCOLOGY, 2016, 63 :38-43
[10]  
Kimura S, 2004, INT J MOL MED, V14, P185