TY - JOUR
T1 - Human papillomavirus type 16 infection and local lymph node metastasis in patients with squamous cell carcinoma
AU - Kawai, Ryoko
AU - Isomura, Madoka
AU - Sato, Nobuaki
AU - Kato, Seeta
AU - Yoshida, Waka
AU - Kamiya, Kei
AU - Nagaya, Yoshitaka
AU - Hattori, Tomofumi
AU - Suzuki, Koji
AU - Funato, Akiyoshi
AU - Yoshiyama, Masanori
AU - Sugita, Yoshihiko
AU - Kubo, Katsutoshi
AU - Maeda, Hatsuhiko
N1 - Publisher Copyright:
© 2016 The Hard Tissue Biology Network Association Printed in Japan, All rights reserved.
PY - 2016/4/12
Y1 - 2016/4/12
N2 - Human papillomavirus (HPV) infection is known to be an independent etiologic factor for oral squamous cell carcinoma (OSCC). Especially, HPV-16 is associated with a significant risk of developing OSCC. The most important prognostic factor in OSCC is local lymph node metastasis (LNM); therefore, knowledge of LNM status is crucial for selecting proper treatment plans. However, it is not clarify relationship between HPV-16 infection and LNM in OSCC. The purpose of this study was to determine the role of HPV-16 infection in LNM in OSCC. We analyzed 130 cases of OSCC (100 cases of OSCC without LNM; 30 cases of OSCC with LNM). HPV-16 infection was detected by PCR, immunohistochemical examination and in situ hybridization. HPV-16 positivity rates among primary tumor (PT) specimens without LNM were 43.0 % (43/100), and HPV-16 positivity rates among PT specimens with LNM were 26.7 % (8/30). In addition, HPV-16 positivity rates in both PT and LNM specimens in 30 OSCC patients with LNM were 10 % (3/30). OSCC with HPV-16 DNA detected by PCR showed positive staining on immunohistochemical examination and in situ hybridization. The HPV-16 infection rate in OSCC with LNM was significantly lower than that for OSCC without LNM. In the case of OSCC with LNM, HPV-16 infection rates for both in PT and LNM were low. This suggests that HPV-16 positive cases had a significantly lower risk of LNM when compared with patients having HPV-16 negative OSCC. The results of the present study suggest that HPV status in OSCC is able to act as a marker for risk of LNM.
AB - Human papillomavirus (HPV) infection is known to be an independent etiologic factor for oral squamous cell carcinoma (OSCC). Especially, HPV-16 is associated with a significant risk of developing OSCC. The most important prognostic factor in OSCC is local lymph node metastasis (LNM); therefore, knowledge of LNM status is crucial for selecting proper treatment plans. However, it is not clarify relationship between HPV-16 infection and LNM in OSCC. The purpose of this study was to determine the role of HPV-16 infection in LNM in OSCC. We analyzed 130 cases of OSCC (100 cases of OSCC without LNM; 30 cases of OSCC with LNM). HPV-16 infection was detected by PCR, immunohistochemical examination and in situ hybridization. HPV-16 positivity rates among primary tumor (PT) specimens without LNM were 43.0 % (43/100), and HPV-16 positivity rates among PT specimens with LNM were 26.7 % (8/30). In addition, HPV-16 positivity rates in both PT and LNM specimens in 30 OSCC patients with LNM were 10 % (3/30). OSCC with HPV-16 DNA detected by PCR showed positive staining on immunohistochemical examination and in situ hybridization. The HPV-16 infection rate in OSCC with LNM was significantly lower than that for OSCC without LNM. In the case of OSCC with LNM, HPV-16 infection rates for both in PT and LNM were low. This suggests that HPV-16 positive cases had a significantly lower risk of LNM when compared with patients having HPV-16 negative OSCC. The results of the present study suggest that HPV status in OSCC is able to act as a marker for risk of LNM.
KW - Human papillomavirus
KW - Lymph node metastasis
KW - Oral squamous cell carcinoma
UR - https://www.scopus.com/pages/publications/84976871896
UR - https://www.scopus.com/pages/publications/84976871896#tab=citedBy
U2 - 10.2485/jhtb.25.115
DO - 10.2485/jhtb.25.115
M3 - Article
AN - SCOPUS:84976871896
SN - 1341-7649
VL - 25
SP - 115
EP - 120
JO - Journal of Hard Tissue Biology
JF - Journal of Hard Tissue Biology
IS - 2
ER -