Review

Article

Oral squamous cell carcinoma: Etiology,

pathogenesis and prognostic value of
genomic alterations
Mehrotra R, Yadav S
Department of Pathology, Moti Lal Nehru Medical College, University of Allahabad, 16/2, Lowther Road,
Allahabad - 211002, India

Correspondence to: Dr. Ravi Mehrotra, E-mail: [email protected]

Abstract
Tumours of the head and neck comprise an important group of neoplasia, the incidence of which is increasing in
many parts of the world. This increase remains high, despite all the advances in modern medicine. This malignancy
is more prevalent in the developing world and unfortunately, has not received satisfactory attention as the more
prevalent cancers of the developed world, like lung, breast, or colon cancer. Recent advances in diagnosis and
therapeutic techniques of these lesions have yielded novel molecular targets, uncovered signal pathway dominance
and advanced early cancer detection. This review covers recent advances in our understanding of the etiology,
molecular changes and the possible role that genomic and proteomic research might play in the diagnosis and
effective cure of this modern-day scourge.
Key words: Oral cancer, apoptosis, telomerase activity, LCM.

More than 95% of the carcinomas of the oral cavity are

of squamous cell type, in nature. They constitute a
major health problem in developing countries,
representing a leading cause of death. The survival
index continues to be small (50%), as compared to the
progress in diagnosis and treatment of other malignant
tumors. According to World Health Organization,
carcinoma of oral cavity in males in developing
countries, is the sixth commonest cancer after lung,
prostrate, colorectal, stomach and bladder cancer, while
in females, it is the tenth commonest site of cancer
after breast, colorectal, lung, stomach, uterus, cervix,
ovary, bladder and liver.[1]
Since, the oral cavity is more accessible to complete
examination, it could be used in early detection of
precancerous and cancerous lesions. But either due to
ignorance or inaccessibility of medical care, the disease
gets detected in the later stages. Thus, there is a need
for improvement in early detection of oral carcinomas,
because in the initial stages, treatment is more effective
and the morbidity is minimal. One method that is
60
60 CMYK

currently being investigated, utilizes in-vivo toluidine

blue staining with oral brush biopsy, for diagnosis of
premalignant lesions, enabling the clinician to choose
the patients for scalpel biopsy.[2]
Most invasive oral carcinomas are preceded by a
preinvasive stage, that may last for many years. Tumor
progression in epithelia has been classified as normal,
hyperplastic (non-dysplastic), dysplastic carcinoma in situ
and invasive carcinoma.[3] The majority of the initial
alterations of precancerous and cancerous oral lesions
are not readily recognizable, on clinical
or histopathological examination. The basic biology of
initiation and progression of these tumors is still
obscure.
Epidemiology and Etiology
Overall incidence and mortality attributed to oral
squamous cell carcinoma (OSCC) is increasing, with
current estimates of age-standardized incidence and
mortality of 6.6/100,000 and 3.1/100,000 in men and
Indian Journal of Cancer | AprilJune 2006 | Volume 43 | Issue 2

Mehrotra, et al.: Oral squamous cell carcinoma

2.9/100,000 and 1.4/100,000 in women, respectively.[1]

Recent studies confirm that oral cancer forms a large
part of the cancer load in parts of India.[4] Tobacco and
alcohol are the two most important known risk factors
for the development of oral cancer. [5] Cofactors in
OSCC include dietary factors, immunodeficiency and
viral infections like HPV 16/18.
Risk factors for oral cancer

The risk factors include tobacco associated intra-oral

carcinogens, which may play a synergistic role in oral
tumorigenesis. From relative risk factors of alcohol and
tobacco, it has been estimated, that 75% of all oral
cancers are preventable. In the remaining 25% of
patients who are not exposed to these substances, the
cause/s of their tumors remains unknown. [6] The
disproportionately higher incidence of carcinoma of the
head-neck in relation to other malignancies in India,
may be due to use of tobacco in various forms,
consumption of alcohol, low socioeconomic condition
related to poor hygiene, poor diet and rampant viral
infections.[7]

times, associated with using the quid, without

tobacco. [8] BQ chewing produces ROS that is
detrimental to oral mucosa and can be directly involved
in tumor initiation process, by inducing mutation, or by
making the mucosa susceptible to BQ ingredients and
environmental toxicants. Betel quid (BQ) chewing
produces reactive oxygen species (ROS), that have
multiple detrimental effects upon the oral mucosa. The
production and release of ROS occurs under alkaline
conditions during the autooxidation of areca nut (AN)
polyphenols, in the BQ chewers saliva.[11] The ROS
can be directly involved in the tumour initiation
process, by inducing genotoxicity and gene mutation, or
by attacking the salivary proteins and oral mucosa,
leading to structural change in the oral mucosa, that
may facilitate the penetration by other BQ ingredients
and environmental toxicants. The nitrosation of areca
alkaloids to AN-specific nitrosamines occurs in the saliva
of BQ chewers.[12] These AN-specific nitrosamines are
mutagenic, genotoxic and capable of inducing tumours
in animal models.[13]
Alcohol

Tobacco
Oral neoplasia has been associated with chewing of
tobacco with betel quid (BQ) in India and other asian
countries, whereas in western countries, cigarette
smoking and heavy alcohol consumption are the main
risk factors.[8] The international agency for research on
cancer (IARC) confirmed that smoking of various
forms of tobacco (e.g., bidis, pipes, cigars and
cigarettes) is carcinogenic in humans. [9] Chewing of
tobacco with BQ increases exposure to carcinogenic
tobacco-specific nitrosamines (TSNA) and to
nitrosamines derived from areca nut alkaloids.
Furthermore, reactive oxygen species (ROS) implicated
in multistage carcinogenesis, are also generated in
substantial amounts in the oral cavity during chewing.
Tobacco smoke pro-carcinogens such as benzo-[]pyrene, are metabolized by oxidizing enzymes,
particularly cytochrome p450, some resulting in the
production of reactive carcinogenic intermediates. Some
studies link that cytochrome P450 family 1, subfamily
A (CYP1A1) and CYP2E1 genotype, shows
susceptibility to oral cancer, but others have failed to
confirm this association.[10]

Alcohol, acting both independently as well as

synergistically with smoking, has been implicated in oral
carcinogenesis.[14] More importantly, alcohol may act as
a solvent and enhance the penetration of carcinogens
into target tissues. Acetaldehyde, which is the alcohol
metabolite, has been identified recently as a tumor
promoter.[15,16]
Viruses
Another risk factor is human papillomavirus (HPV),
which is also closely associated with benign and
malignant oral lesions. This virus is detected in
condylomas, focal epithelial hyperplasia, squamous cell
papilloma and malignant oral lesions. HPV positivity is
higher in tumors from the oral cavity (59%), pharynx
(43%) and larynx (33%).[17] Among those, only a small
fraction of HPV-infected lesions rarely proceed to
malignant transformation, specially those with HPV
subtypes 16,18.[18-21] Hence, these studies indicate that
tumorigenic conversion requires the presence of other
risk factors.
Diet

Betel Quid and Areca Nut

Betel chewing is reported to be the most important
etiological factor in oral submucous fibrosis. The use of
betel quid, containing both areca nut and tobacco, is
associated with a much higher relative risk of oral
cancer, between 8-15 times as compared to that of 1-4
Indian Journal of Cancer | AprilJune 2006 | Volume 43 | Issue 2

The importance of diet and nutrition in oral neoplasia

has been indicated in several epidemiological
studies.[22,23] Fruits and vegetables (high in vitamins
A and C) are described as protective in oral neoplasia,
whereas meat and red chilli powder are thought to be
risk factors. Although the individual micronutrients
61
CMYK61

Mehrotra, et al.: Oral squamous cell carcinoma

responsible have not been formally identified, vegetables

and fruits that protect against oral cancer and precancer,
are rich in b-carotene, vitamin C and vitamin E, with
anti-oxidant properties. Iron deficiency, resulting in oral
epithelial atrophy and the Plummer-Vinson (Patterson
Brown Kelly) syndrome, is associated with cancer of
upper air and food passages and dietary iron may play
a protective role in maintaining the thickness of the
epithelium.[24]
Family History of Head and Neck Squamous Cell
Carcinoma (HNSCC)
Epidemiological evidence from case-control studies of
HNSCC, indicates that a family history of head and
neck cancer is a risk factor. The ability to repair DNA
damaged by tobacco carcinogens, such as benzo-[]pyrene diol epoxide, is defective in some patients with
head and neck cancer. Head and neck cancer patients
show an increased susceptibility to chromosome damage
by mutagens.[25]
Villaret et al used cDNA array and identified genes
such as keratin 17 and 19, laminin-5, connexin-26 and
VEGF as being differentially expressed in HNSCC
tissues, with respect to normal tissue.[26]
Immune Deficiency
A defective immune response, as seen in a human
immunodeficiency virus (HIV)-infected individual, may
predispose to cancer. The commonest oral malignancy
in HIV-infected patients is Kaposis sarcoma[27] and the
Human Herpes virus type 8 (HHV-8) has been
implicated as the aetiological agent. [28] Lymphoma,
mostly non-Hodgkin B cell lymphoma in HIV-infected
individuals, or other immunosuppressed states, is
commonly associated with Epstein-Barr virus and may
occur in the head and neck. Oral squamous cell
carcinomas of the lip are more common in transplant
recipients receiving immunosuppressive therapy, but
HIV infection does not predispose to intra-oral
squamous cell carcinoma.[29]
Candida

Candida albicans can induce epithelial proliferation and

can produce carcinogens from procarcinogens in vitro.
Chronic hyperplastic candidosis presents as nodular or
speckled-white mucosal plaques. They are potentially
malignant oral epithelial lesions.[30]
Molecular Changes in Oral Cancer
Cancer occurs through multiple steps, each characterized
by the sequential stimulation of additional genetic
62
62 CMYK

defects, followed by clonal expansion. The genetic

alterations observed in head and neck cancer are mainly
due to oncogene activation and tumor suppressor gene
inactivation, leading to deregulation of cell
proliferation and death. These genetic alterations,
include gene amplification and overexpression of
oncogenes such as myc, erbB-2, Epidermal Growth
Factor Receptor (EGFR), cyclin D1 and mutations,
deletions and hypermethylation leading to p16 and p53
tumor suppressor gene inactivation.[31]
Tumor Suppressor Genes (TSGs) and Growth
Regulators
Growth regulators and TSGs act as transducers of
negative growth signals. Genetic alterations involving
the tumor suppressor genes p16 and p53, are frequently
observed in head and neck tumors. Genetic
abnormalities inactivating the p16 gene might confer
cell growth defects, contributing to the tumorigenic
process. These genes are involved in cell cycle
regulation, including cell cycle arrest and apoptosis.
Alteration in both alleles of a gene is required for the
loss of function. The TSG p53, is called as Guardian of
the Genome, having a role in maintaining genomic
stability, cell cycle progression, cellular differentiation,
DNA repair and apoptosis.[32] A number of findings
indicate that p53 plays an important role in cell-cycle
control (both G1/S and G2/M checkpoints) and in the
induction of apoptosis. The gene can be inactivated by
several mechanisms, including point mutations, deletions
and binding with cellular and viral proteins. p53 geneinactivation via the above mentioned factors, has been
demonstrated in squamous cell carcinoma. Due to its
high catabolic rate, it is not usually possible to
demonstrate p53 protein in normal tissues using
immunohistochemical procedures, whereas mutated p53
exhibits a much lower catabolic rate and accumulates in
the cells.
Genomic instability

The evaluation of the genomic stability can be done

using techniques such as Loss of heterozygosity (LOH)
screening and comparative genomic hybridization
(CGH). Loss of heterozygosity of the p53 allele has
been reported in 20% of OSCCs, as well as in 22% of
premalignant oral lesions. [33] The risk of progression
from premalignancy to cancer is low, when no genetic
changes were seen, intermediate, if there is genetic loss
on the short arms of chromosomes 3 and 9 (3p and
9p) and high, if there is 3p and 9p loss accompanied
by genetic loss on additional chromosome arms,
including 4q, 8p, 11q, 13q and 17p. The LOH of the
H-ras allele may encompass a tumor suppressor gene in
the vicinity of the oncogene. Loss of chromosome 11
Indian Journal of Cancer | AprilJune 2006 | Volume 43 | Issue 2

Mehrotra, et al.: Oral squamous cell carcinoma

alleles has been reported in a number of tumors. These

techniques can be used to identify and confirm both
known and unknown alterations (deletions, mutations)
in the genomes of a variety of human tumors. EGFR
and its ligands have been studied extensively in OSCCs.
Over expression of EGFR and Transforming growth
Factor (TGF) has been found to be associated with a
decrease in the disease-free and cause-specific survival
rates. [33] TGF-m-RNA was found at 5 times higher
levels in 96% of histologically normal tissues examined
from patients with OSCCs and at 5 times higher levels
in 87.5% of tumors when compared with normal
mucosa.[34]
Role of deregulated apoptosis in the pathogenesis of
oral cancer

The deregulation of apoptosis-related genes, aids in

successful carcinogenesis. The relative contribution of
apoptosis and proliferation to disease progression in the
oral mucosa, was examined using terminal
deoxynucleotidyl transferase nick end-labeling (TUNEL)
assay and Ki-67 staining. Further apoptosis related cell
cycle regulators, namely Retinoblastoma (Rb), cyclin
D1 and Fragile histidine triad gene (FHIT) were
analyzed for Loss of heterozygosity (LOH), gene
amplification and aberrant transcripts, respectively in
oral cancer samples. Status of p53, bcl-2 and bax,
members of the p53 dependent apoptotic pathway, were
evaluated in oral cancers/oral lesions by
immunohistochemistry. Frequent overexpression of
apoptosis regulators p53, bcl-2 and bax, was observed
in oral cancers and in a subset of oral lesions. It was
further revealed that there is overexpression of antiapoptotic members of the bcl-2 family namely, bclxL
and Mcl-1, in oral cancer cell lines. These studies thus
indicate, that evasion of apoptosis via abnormal
expression of bcl-2, bclxL, mcl-1 and p53, may
contribute to oral cancer pathogenesis.[35]
Enhanced telomerase activity

The structures at the ends of eukaryotic chromosomes

are termed Telomeres. As telomeres are lost during
cell divisions, the chromosomal ends are no longer
protected, which leads to the fusion of the
chromosomes and karyotypic abnormalities, that
eventually cause cell death. The ribonucleoprotein
enzyme telomerase extends the telomeric repeat
sequences at the chromosomal ends; and it is active in a
majority (90%) of human neoplasia, but inactive in
most normal cells.[36] Mao et al analyzed 16 HNSCC
cell lines, 29 tumor specimens and adjacent normal and
dysplastic mucosa; and did not find telomerase activity
in any of the normal tissues, but it was found in 100%
of the cell lines, 90% of the invasive neoplasia and
100% of the dysplastic lesions.[37] Other reports also
Indian Journal of Cancer | AprilJune 2006 | Volume 43 | Issue 2

confirm high telomerase activity in oral tumors[38] and

in 37% of OSCC patients, using oral rinses.[39]
Neovascularization
Angiogenesis, defined as the growth of new blood
vessels (neovascularization) from pre-existing ones, is a
complex process, absolutely needed for the continued
growth and survival of solid neoplasia. This process of
angiogenesis is in itself a multi-step process, that
appears to be regulated by both stimulatory and
inhibitory factors. [40] The steps critical to successful
angiogenesis, include the degradation of the extracellular
matrix, endothelial cell proliferation, migration and
assembly of endothelial cells into higher order
structures. In the majority of cancers, highly
vascularized tumors showed a poor prognosis and the
influence of tumor angiogenesis proved to be
independent of conventional prognostic indicators.[41]
Cytokine profile

Suppression of Th1 cytokine genes, was reported due to

increase in tumor load and lymph node invasion, which
skewed it towards a Th2-like cytokine response.
Mehrotra et al have earlier reported that HNSCCs, but
not benign lesions, express Interleukin-4 receptors in
situ[42] and Interleukin-13 was secreted by HNSCCs, but
does not modulate their growth in vitro. It has been
postulated that these cytokines, in addition to others,
were responsible for the growth pattern of these tumors
and could be responsible for their active spread.[43]
Proteomics and array technology

Oncologic research during the past decade, relied on the

use of genomic tools and now, in the post genomic era,
there is a strong drive towards proteomics. Genomics
and proteomics studies are used for the molecular
classification of tumors and the identification of markers
for the early detection of cancer. The National Cancer
Institute, Bethesda, USA has successfully completed the
Cancer genome anatomy project (CGAP), with the goal
of achieving a comprehensive molecular characterization
of normal, pre-cancerous and malignant cells, to create a
complete profile of genes expressed during cancer
development.[44]
The term Proteomics indicates proteins expressed by a
genome and is the systematic analysis of protein profiles
of tissues. In a recent report, an oral cancer-specific
human Bacterial artificial chromosome (BAC) array,
called the oral cancer genomic regional array (OCGR),
has also been described to detect copy number
alterations in OSCC.[45] BAC array CGH is similar to
conventional chromosomal CGH, except that it uses
segments of human DNA as hybridization targets,
63
CMYK63

Mehrotra, et al.: Oral squamous cell carcinoma

instead of a metaphase spread of chromosomes.

Hybridization on to such arrays, overcomes the low
resolution that limits conventional CGH. As with
conventional CGH, total genomic DNA from a tumor
and a normal cell population are differentially labeled
and co-hybridized onto an array. The ratio of the
fluorescence intensities on each DNA spot on the array
is proportional to the copy number of the
corresponding sequence. High-resolution arrays allow
for the delineation of amplification and deletion
boundaries, in a single experiment.
These arrays have been instrumental in detailed analysis
of specific chromosomal regions. Mendez et al examined
the genetic expression profiles of 26 invasive squamous
cell carcinomas of the oral cavity and oropharynx, 2
premalignant lesions and 18 normal oral tissue samples,
using oligonucleotide arrays representing approximately
7000 human genes and found many genes to be up
and down regulated, thus helping to differentiate the
premalignant from the malignant tissues.[45]
Leethanakul et al c o m p a red the gene expression
profiles of five laser- microdissected head and neck
squamous cell carcinioma (HNSCC) specimens, with
those of their matching normal tissues.[46] In the study,
human cancer cDNA membrane arrays from Clontech
USA were used, containing DNA fragments in
duplicate, for 588 known human cancer genes.
Interestingly, the genes expressed differentially in the
invasive specimens compared with their corresponding
normal tissues and included those involved in the
control of cell growth and differentiation, angiogenesis,
apoptosis, cell cycle and signaling, most of which have
not been previously described in HNSCC. Belbin et al,
have identified 375 genes that demonstrated significant
expression differences and divided the patients with
HNSCCs into clinically distinct subgroups, based on
gene expression patterns found and outcome could be
predicted.[47]
The development of high throughput hybridisation
based methods, such as cDNA and oligonucleotide
microarrays, allows the simultaneous analysis of gene
expression alterations in thousands of genes, in HNSCC.
These studies have used a variety of experimental
designs, tumour types, array platforms and statistical
tools, making direct comparisons of results difficult.
However, the potential biological and clinical
implications of gene expression signatures of HNSCC in
tumour classification, prognosis and treatment, are
enormous.[48]
Another approach using Polymerase chain reaction
64
64 CMYK

differential display technique, has been applied by

Lemaire et al.[49] Contrary to the microarrays, wherein
analysis is limited to the set of genes printed on the
array, the Polymerase chain reaction differential display
technique has the advantage of randomly sampling the
whole transcriptome. Using this technique, the authors
were able to identify novel expressed sequences, that did
not correspond to known genes, which could be
potential tumor markers and targets for drug design in
HNSCC.
New evidence for new gene expression- based
biomarkers of local treatment failure in the head and
neck cancers, was reported recently by Ginos et al, who
studied gene expression profile in 41 cases and found
2890 genes associated with extracellular matrix
production, proliferation, cytokine/chemokine expression,
immune response, invasion and metastasis that showed
significant differences in their expression.[50] Another
new protein analysis system based on the surface
enhanced laser desorption/Ionization (SELDI), has been
recently applied for the separation, detection and
analysis of multiple proteins in a very small amount
(~10ng) of micro-dissected cancer tissue. This
technique facilitates protein capture, purification, analysis
and processing from complex biological mixtures,
directly onto protein chip array surfaces and the
detection of the purified proteins is performed by Time
of Flight Mass Spectrometry, (TOF-MS). A major
feature in SELDI-TOF MS, is its ability to provide a
rapid protein expression profile.[51]
Laser Capture Microdissection (LCM)
This novel technology offers sample purity and
complements gene chips, by allowing accurate gene
profiling studies. The method of LCM has made the
study of cancer biology and other areas of cell biology,
more precise and has greatly boosted the current efforts
in defining the molecular basis of malignancy, as they
exist in vivo.[42] The microenvironment of a carcinoma
consists not only of the malignant epithelial component,
but also the surrounding stroma and normal tissue.
These distinct microcompartments use receptors, cell
junctions and inter and intracellular signaling molecules,
to allow tumor cells to communicate with their
surroundings and play an active role in their own
control or progression. LCM provides an ideal method
for the extraction of cells from specimens, in which the
exact morphologies of both the captured cells and the
surrounding tissue, are preserved. When rapid
immunohistochemical staining techniques are combined
with LCM, we can get more accurate microdissection
of cell subsets.[52]
Indian Journal of Cancer | AprilJune 2006 | Volume 43 | Issue 2

Mehrotra, et al.: Oral squamous cell carcinoma

New Therapies

References

Management of cancer remains difficult, in spite of

considerable advances in understanding the molecular
biology of oral cancer and still we bank upon
radiotherapy and chemotherapy. Although more than
1500 anticancer agents are in active development, with
over 500 in clinical trials, still there is a desperate need
for more effective and less toxic therapies. Therapeutic
agents targeted specifically at patients with head and
neck cancer, include the family of tyrosine-kinase
inhibitors in particular, the epidermal growth factorreceptor (EGFR) and cyclin dependent kinase (CDK)
inhibitors. Promising gene therapy strategies have been
reported on the use of highly efficient adenovirus
vectors, to deliver therapeutic genes in advanced cases
of HNSCC. A prime example is ONYX-015, which is
an adenovirus with the EIB55-kDa gene deleted, to
selectively replicate in and lyse p53-deficient cancer cells,
while sparing normal cells. A combination of
intratumoural ONYX-015 injection with Cisplatin and
5-Flourouracil in patients, suggests that it is effective
and that the response at injected tumor sites is
durable.[53] Irressa is an orally-active selective epidermal
growth factor receptor-tyrosine kinase inhibitor, showing
anti-tumor activity in HNSCC, in combination with
radiation treatment.[54]

1.
2.

3.
4.

5.

6.
7.

8.

9.

10.
11.

12.

Onco-chips are the new concept consisting of several

reliable diagnostic head and neck cancer markers, which
may be used to diagnose cancer. The treatment of cells
with therapeutic chemicals, has been shown to produce
specific changes in gene expression and owing to the
costly nature of clinical trials involved, much effort by
pharmaceutical companies is being invested into Toxo
chips, which may contain the relevant probes to study
cell expression responses to chemical or drug insult,
during drug development.[54]

13.

14.

15.
16.

Conclusion
17.

The global increase in frequency and mortality, as well

as the poor prognosis of head and neck squamous cell
carcinoma, has intensified current research efforts in the
field of prevention and early detection of this disease.
The advances in the understanding of the molecular
basis of HNSCC should help in the identification of
new markers. The study of the carcinogenic process of
the head and neck, including continued analysis of new
genetic alterations, along with their temporal sequencing
during initiation, promotion and progression, will allow
us to identify new diagnostic and prognostic factors,
which will provide a promising basis for the application
of more rational and efficient treatments.
Indian Journal of Cancer | AprilJune 2006 | Volume 43 | Issue 2

18.

19.

20.
21.

22.

Landis SH, Murray T, Bolden S, Wingo PA, Cancer statistics, 1999.

CA Cancer J Clin 1999;49:8-31.
Mehrotra R, Gupta A, Singh M, Ibrahim R. Application of cytology
and molecular biology in diagnosing premalignant or malignant
oral lesions. Mol Cancer 2006;5:11.
Meyskens FL. Biology and intervention of premalignant process.
Can Bull 1991;43:475-80.
Sunny L, Yeole BB, Hakama M, Shiri R, Sastry PS, Mathews S, et
al. Oral cancers in Mumbai, India: A fifteen years perspective with
respect to incidence trend and cumulative risk. Asian Pac J Cancer
Prev 2004;5:294-300.
Daftary DK, Murti PR, Bhonsle RB, et al. Risk factors and risk
markers for oral cancer in high incidence areas of the world. In:
Johnson NW, editor. Oral Cancer, Vol. 2. Cambridge University
Press: Cambridge; 1991. p. 29-63.
Walker DM, Boey G, McDonald LA. The pathology of oral cancer.
Pathology 2003;35:376-83.
Franceschi S, Bidoli P, Herrero R, Munoz N. Comparison of cancers
of the oral cavity and pharynx world wide:etiological clues. Oral
Oncol 2000;36:106-15.
Manjari M, Popli R, Paul S, Gupta VP, Kaholon SK. Prevalence of
oral cavity, pharynx, larynx and nasal cavity malignancies in
Amritsar, Punjab. Indian J Otolar yngol Head Neck Surg
1999;48:191-5.
International Agency for Research on Cancer (IARC). Tobacco
smoking. IARC Monograph on the evaluation of carcinogenic risks
of chemicals to humans. IARC: Lyon, France; 1986. p. 1-421.
Kawajiri K, Fujii-Kuriyama Y. P450 and human cancer. Jpn J Cancer
Res 1991;82:1325-35.
Merchant A, Husain SS, Hosain M, Fikree FF, Pitiphat W, Siddiqui
AR, et al. Paan without tobacco: An independent risk factor for
oral cancer. Intl J Cancer 2000;86:128-31.
Nair J, Ohshima H, Friesen M, Croisy A, Bhide SV, Bartsch H.
Tobacco-specific and betel nut-specific N-nitroso compounds:
Occurrence in saliva and urine of betel quid chewers and formation
in vitro by nitrosation of betel quid. Carcinogenesis 1985;6:295303.
Prokopczyk B, Rivenson A, Bertinato P, Brunnemann KD,
Hoffmann D. 3-(Methylnitrosamino) propionitrile: Occurrence in
saliva of betel quid chewers, carcinogenicity and DNA methylation
in F344 rats. Cancer Res 1987;47:467-71.
International Agency for Research on Cancer (IARC). Alcohol
drinking. IARC Monograph on the evaluation of carcinogenic risks
of chemicals to humans. IARC: Lyon, France; 1989. p. 1-416.
Blot WJ. Alcohol and cancer. Cancer Res 1992;52:2119s-23s.
Harty LC, Caporaso NE, Hayes RB, Winn DM, Bravo-Otero E, Blot
WJ, et al. Alcohol dehydrogenase 3 genotype and risk of oral cavity
and pharyngeal cancers. J Natl Cancer Inst 1997;89:1698-705.
Gillison ML, Koch WM, Capone RB, Spafford M, Westra WH, Wu
L, et al. Evidence for a causal association between human
papillomavirus and a subset of head and neck cancers. J Natl
Cancer Inst 2000;92:709-20.
McKaig RG, Baric RS, Olshan AF. Human papillomavirus and head
and neck cancer: Epidemiology and molecular biology. Head Neck
1998;20:250-65.
DiPaolo JA, Woodworth CD, Popescu NC, Koval DL, Lopez JV,
Doniger J. HSV-2 induced tumorigenicity in HPV-16-immortalised
human genital keratinocytes. Virology 1990;177:777-9.
Scully C. New aspects of oral viral diseases. Curr Top Pathol
1996;90:29-96.
Scully C. Oral squamous cell carcinoma; From a hypothesis about
a virus, to concern about possible sexual transmission. Oral Oncol
2002;38:227-34.
McLaughlin JK, Gridley G, Block G, Winn DM, Preston-Martin S,
Schoenberg JB, et al. Dietary factors in oral and pharyngeal cancer.
J Natl Cancer Inst 1988;80:1237-43.

65
CMYK65

Mehrotra, et al.: Oral squamous cell carcinoma

23.

24.

25.

26.

27.

28.

29.

30.
31.

32.
33.

34.

35.

36.
37.

38.

39.

De Stefani E, Deneo-Pellegrini H, Mendilaharsu M, Ronco A. Diet

and risk of cancer of the upper aerodigestive tract-I. Foods. Oral
Oncol 1999;35:17-21.
Negri E, Franceschi S, Bosetti C, Levi F, Conti E, Parpinel M, et al.
Selected micronutrients and oral and pharyngeal cancer. Int J
Cancer 2000;86:122-7.
Spitz MR, Fueger JJ, Beddingfield NA, Annegers JF, Hsu TC, Newell
GR, et al. Chromosome sensitivity to bleomycin induced
mutagenesis an independent risk factor for upper aerodigestive
tract cancer. Cancer Res 1989;49:4626-8.
Villaret DB, Wang T, Dillon D, Xu J, Sivam D, Cheever MA, et al.
Identification of genes over expressed in head and neck squamous
cell carcinoma using a combination of complementary DNA
subtraction and microarray analysis. Laryngoscope
2000;110:374-81.
Scully C, Laskaris G, Pindborg J, Porter SR, Reichart P. Oral
manifestations of HIV and their management. I. More common
lesions. Oral Surg Oral Med Oral Pathol 1991;71:158-66.
Flaitz CM, Hicks MJ. Role of lymphotrotrophic herpesvirus in
malignancies associated with immunosuppressed states. In:
Millard HD, Mason DK, editors. Perspectives on the 1998 3rd
World Workshop on Oral Medicine. University of Michigan Press:
Ann Arbor, MI; 2000.
Harris JP, Penn I. Immunosuppression and the development of
malignancies of the upper airway and related structures.
Laryngoscope 1981;91:520-8.
Cawson RA. Leukoplakia and oral cancer. Proc R Soc Med
1969;62:610-4.
Mehrotra R, Vasstrand EN, Ibrahim SO. Recent advances in
understanding carcinogenicity of oral squamous cell carcinoma:
From basic molecular biology to latest genomic and proteomic
findings. Cancer Gen Proteom 2004;1:283-94.
Weinberg RA. Tumor suppressor genes. Science 1991;254:113846,52.
Schepman KP, van der Waal I. A proposal for classification and
staging system for oral leukoplakia: A preliminary study. Oral
Oncol 1995;31B:396-8.
Grandis JR, Tweardy D. Elevated levels of transforming growth
factor alpha and epidermal growth factor receptor messenger
RNA are early markers of carcinogenesis in head and neck cancer.
Cancer Res 1993;53:3579-84.
Teni TR, Pawar SN, Mallick S. Expression of Apoptosis related
genes in human oral cancers from India. 3 rd World assembly on
tobacco counters health, Book of Abstracts: 2004. p. 36.
Reddel RR. Alternative lengthening of telomeres, telomerase and
cancer. Cancer Lett 2003;194:155-62.
Mao L, Lee JS, Fan YH, Ro JY, Batsakis JG, Lippman S, et al.
Frequent microsatellite alterations at chromosomes 9p21 and
3p14 in oral premalignant lesions and their value in cancer risk
assessment. Nat Med 1996;6:682-5.
Miyoshi Y, Tsukinoki K, Imaizumi T, Yamada Y, Ishizaki T, Watanabe
Y, et al. Telomerase activity in oral cancer. Oral Oncol
1999;35:283-9.
Califano J, Ahrendt SA, Meininger G, Westra WH, Koch WM,

66
66 CMYK

40.
41.
42.

43.

44.

45.

46.

47.

48.

49.

50.

51.

52.

53.

54.

Sidransky D. Detection of telomerase activity in oral rinses from

head and neck squamous cell carcinoma patients. Cancer Res
1996;56:5720-2.
Bergers G, Benjamin LE. Tumorigenesis and the angiogenic switch.
Nat Rev Cancer 2003;3:401-10.
Kerbel RS. Tumor angiogenesis: Past, present and the near future.
Carcinogenesis 2000;21:505-15.
Mehrotra R, Varricchio F, Husain SR, Puri RK. Head and neck
cancers, but not benign lesions, express interleukin-4 receptors
in situ. Oncol Rep 1998;5:45-8.
Mehrotra R. Interleukin 13 is secreted by human head and neck
tumours and does not modulate their growth in vitro. Indian J Exp
Biol 1998;36;805-7.
Shillitoe EJ, May M, Patel V, Lethanakul C, Ensley JF, Strausberg
RL, et al. Genome-wide analysis of oral cancer-Early results from
the Cancer Genome Anatomy Project. Genome Anatomy Project.
Oral Oncol 2000;36:8-16.
Garnis C, Campbell J, Zhang L. Rosin MP, Lam WL. OCGR array:
An oral cancer genomic regional array for comparative genomic
hybridization analysis. Oral Oncol 2004;40:511-9.
Leethanakul C, Patel V, Gillespie J, Pallente M, Ensley JF,
Koontongkaew S, et al. Distinct pattern of expression of
differentiation and growth-related genes in squamous cell
carcinomas of the head and neck revealed by the use of laser
capture micro dissection and cDNA arrays. Oncogene
2000;19:3220-4.
Belbin TJ, Singh B, Barber I, Socci N, Wenig B, Smith R, et al.
Molecular classification of head and neck squamous cell carcinoma
using cDNA microarrays. Cancer Res 2002;62:1184-90.
Mendez E, Cheng C, Farwell DG, Ricks S, Agoff SN, Futran ND, et
al. Transcriptional expression profiles of oral squamous cell
carcinomas. Cancer 2002;95:1482-94.
Lemaire F, Millon R, Young J, Cromer A, Wasylyk C, Schultz I, et
al. Differential expression profiling of head and neck squamous
cell carcinoma (HNSCC). Br J Cancer 2003;86:1940-9.
Ginos MA, Page GP, Michalowicz BS, Patel KJ, Volker SE,
Pambuccian SE, et al. Identification of a gene expression signature
associated with recurrent disease in squamous cell carcinoma of
the head and neck. Cancer Res 2004;64:55-63.
Marvin LF, Roberts MA, Fay LB. Matrix-assisted laser desorption/
ionization time-of-flight mass spectrometry in clinical chemistry.
Clin Chim Acta 2003;337:11-21.
Fend F, Emmert-Buck MR, Chuaqui R, Cole K, Lee J, Liotta LA et
al. Immuno-LCM: Laser capture micro dissection of
immunostained frozen sections for mRNA analysis. Am J Pathol
1999;154:61-6.
Khuri FR, Nemunaitis J, Ganly I, Arseneau J, Tannock IF, Romel L,
et al. A controlled trial of intratumoral ONYX-015, a selectively
replicating adenovirus, in combination with cisplatin and 5fluorouracil in patients with recurrent head and neck cancer.
Nature Med 2000;6:879-85.
Dykxhoorn DM, Novina CD Sharp PA. Killing the messenger: Short
RNAs that silence gene expression. Nat Rev Mol Cell Biol
2003;4:457-67.

Indian Journal of Cancer | AprilJune 2006 | Volume 43 | Issue 2