Gene silencing in Breast cancer

S
Santhi DasariASSISTANT PROFESSOR en KRISHNA UNIVERSITY
VIJAYA INSTITUTE OF PHARMACEUTICAL
SCIENCES FOR WOMEN
GENE SILENCING IN
UNDER THE GUIDENCE OF
Mrs D . Santhi Krupa
Assistant . Professor
Dept. of Pharmacology
Presented by
S . Anusha
IV B Pharmacy
137N1R0078
CONTENTS
 Introduction
 Classification of breast cancer
 Epidemiology
 Symptoms
 Etiology/epidemiologic risk factors
 Anatomy of the breast
 Pathology
 Stages of breast cancer
 Breast cancer and pregnancy
 Diagnosis and screening
 Treatment
 Early detection
 Conclusion
INTRODUCTION
 Breast cancer is characterised by the uncontrolled growth of
abnormal cells in the milk producing glands of the breast or in the
passages (ducts) that deliver milk to the nipples.
 Breast Cancer , the second-leading cause of cancer deaths in
women , is the disease women fear most.
 Breast Cancer can also occur in men, but it’s far less common.
 In the last 30 years, doctors have made great studies in early
diagnosis and treatment of the disease and in reducing breast
cancer deaths.
 80% of breast cancers occur in women older than age 50.In
30s,have a one in 233 chance of developing breast cancer. By
age 85 , chance is one in eight.
 In 1975 a diagnosis of breast cancer usually meant radical
mastectomy –removal of the entire breast along with under arm
lymph node and muscles underneath the breast.
CLASSIFICATION
 Based on histological appearance
 Ductal Carcinoma in situ (DCIS)
 Infiltrating or invasive Ductal carcinoma (IDC)
 Medullary carcinoma
 Lobular Carcinoma in situ (LCIS)
 Infiltrating Lobular Carcinoma
 Infiltrating Lobular Carcinoma
 Mucillus carcinoma or colloid
 Paget’s disease
 Inflammatory breast cancer
 Metastatic breast cancer
 Triple negative breast cancer
EPIDEMIOLOGY
 Breast cancer constitutes a major public health issue , resulting
in over 4,00,000 annual deaths and about 4.4 million women
living with this disease.
 It accounts for 16% of all female cancers and 22.9% of
invasive cancers in women.
 18.2% of all cancer deaths in world wide, including both males
and females, are from breast cancer.
 There is an international/geographical variation in the
incidence of breast cancer.
 Incidence rates are higher in the developed countries than in
the developing countries and japan.
SYMPTOMS
 A lump in a breast
 A pain in the armpits or breast that does
not seem to be related to the woman's
menstrual period
 Redness of the skin of the breast
 A rash around (or on) one of the nipples
 A swelling (lump) in one of the armpits
 An area of thickened tissue in a breast
 One of the nipples has a discharge;
sometimes it may contain blood
 The size or the shape of the breast
changes
 The nipple-skin or breast-skin may have
started to peel, scale or flake.
RISK FACTORS FOR BREAST CANCER
Non-modifiable
 Gender
 Age(>45y)
 Genetic changes of breast
cancer
 Family history of breast cancer
 Female Personal history of
breast cancer
 Race and ethnicity
 Dense breast tissue
 Lobular carcinoma in
situ(LCIS)
 Menstrual periods
 Diethyl still besterol exposure
 Previous chest radiation
Modifiable
 Not having children
 Contraceptives
 Harmone therapy after
menopause
 Alcohol consumption
 Breast feeding
 Obesity
 Physical exercise
ETIOLOGY
 General
Aging
Gender
 Genetics
Family history
Inherited factors
 Body
Obesity
Not having children
High breast density
Certain breast changes
Menstrual history
 Life style
A sedentary life style
Heavy drinking
ANATOMY OF BREAST CANCER
PATHOLOGY OF BREAST CANCER
 Hereditary cancers are primarily
caused by an inherited genetic
defect.
 Less than 0.3% of the population
are carriers of a genetic mutation
that has a large effect on cancer
risk and these cause less than
3–10% of cancer.
 Some of
these syndromes include certain
inherited mutations in the
genes BRCA1 and BRCA2 with
a more than 75% risk of breast
cancer and ovarian cancer,
and Hereditarynonpolyposiscolor
ectal cancer (HNPCC or Lynch
syndrome).
 GENETICS  EPIGENETICS
PATHOPHYSIOLOGY OF BREAST CANCER
STAGES OF BREAST CANCER
STAGES DESCRIPTION
Stage-0
• Abnormal cells in the lining of the ducts(or) sections of
the breast.
• Results in increased risk of developing cancer in both
breasts.
Stage-1 • Invasive breast cancer , the cancerous cells are
breaking through to or invading surrounding normal tissue.
Stage-2a
2b
• No tumour but there are cancerous cells in the lymph
nodes , or there is a tumour that has grown.
• Cancerous cells in the lymph nodes and/or tumour has
grown.
Stage-3 • Cancer has spread to lymph nodes near breastbone and
chest wall.
Stage-4 • Cancer has spread to other parts
BREAST CANCER AND PREGNANCY
Breast cancer and pregnancy can be classified into three main
situations; these are
(a) breast cancer that is detected during the evolution of pregnancy
(b) breast cancer that is detected during lactation or postpartum, and
(c) pregnancy in patients who have had a previous breast cancer.
Cancer complicates approximately 1 per 1000 pregnancies
and accounts for one-third of maternal deaths during gestation.
The prevalence of breast cancer during pregnancy is increasing
due to delayed onset of childbearing.
DIAGNOSIS OF BREAST CANCER
 PHYSICAL EXAM AND HISTORY:
 MAMMOGRAM
 ULTRASOUND EXAM
 MRI (MAGNETIC RESONANCE IMAGING)
 BLOOD CHEMISTRY STUDIES:
 BIOPSY:
 Excisional biopsy
 Incisional biopsy
 Core biopsy
 Fine-needle aspiration (FNA) biopsy
 Biopsy samples are tested for the following
 ESTROGEN AND PROGESTERONE
RECEPTOR TEST
 HUMAN EPIDERMAL GROWTH FACTOR
TYPE 2 RECEPTOR(HER2/neu)TEST
 MULTIGENE TESTS
DIGITAL MAMMOGRAPHY
MAMMOGRAPHY
SCREENING
 Average –size lump found by women practicing
occasional breast self exam.
 Average –size lump found by women practicing
regular breast self exam.
 Average –size lump found by first mammogram.
 Average –size lump found by getting regular
mammograms.
TREATMENT OF BREAST CANCER
 Surgery
Breast conserving or mastectomy , with lymph node
examination(ALND or SLNB)
 Chemotherapy
Before or after surgery. Anthracyclins, Taxanes etc
 Hormonal therapy
SERMs, Als, LHRH analogues, oophrectomy
 Targeted biological therapy
Tratuzumab, new dual therapies very promising
 Radiotherapy
Teletherapy , brachytherapy, intraop RT (TARGIT trail)
MANAGEMENT OF BREAST CANCER
EARLY DETECTION
 Early detection of breast cancer plays the leading
role in reducing mortality rates and improving the
patient’s prognosis(Elmore et al.,2005)
 The survival rate is higher with early detection of
breast cancer. However, with local invasion, the
survival rate decreases and if it is diagnosed at the
latest stage, only a very low numbers of patients
will survive.
 For primary prevention of breast cancer, women
need to be adequately informed about risk factors
and risk reduction strategies of breast cancer.
CONCLUSION
Management of breast cancer is a major
challenge in resource limited countries. Efforts
should be geared towards early diagnosis, prompt
and standardized treatment to reduce the burden of
advanced disease in women, majority of who are
worse hit in the most productive part of their life
time.
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Gene silencing in Breast cancer

  • 1. VIJAYA INSTITUTE OF PHARMACEUTICAL SCIENCES FOR WOMEN GENE SILENCING IN UNDER THE GUIDENCE OF Mrs D . Santhi Krupa Assistant . Professor Dept. of Pharmacology Presented by S . Anusha IV B Pharmacy 137N1R0078
  • 2. CONTENTS  Introduction  Classification of breast cancer  Epidemiology  Symptoms  Etiology/epidemiologic risk factors  Anatomy of the breast  Pathology  Stages of breast cancer  Breast cancer and pregnancy  Diagnosis and screening  Treatment  Early detection  Conclusion
  • 3. INTRODUCTION  Breast cancer is characterised by the uncontrolled growth of abnormal cells in the milk producing glands of the breast or in the passages (ducts) that deliver milk to the nipples.  Breast Cancer , the second-leading cause of cancer deaths in women , is the disease women fear most.
  • 4.  Breast Cancer can also occur in men, but it’s far less common.  In the last 30 years, doctors have made great studies in early diagnosis and treatment of the disease and in reducing breast cancer deaths.  80% of breast cancers occur in women older than age 50.In 30s,have a one in 233 chance of developing breast cancer. By age 85 , chance is one in eight.  In 1975 a diagnosis of breast cancer usually meant radical mastectomy –removal of the entire breast along with under arm lymph node and muscles underneath the breast.
  • 5. CLASSIFICATION  Based on histological appearance  Ductal Carcinoma in situ (DCIS)  Infiltrating or invasive Ductal carcinoma (IDC)  Medullary carcinoma  Lobular Carcinoma in situ (LCIS)  Infiltrating Lobular Carcinoma  Infiltrating Lobular Carcinoma  Mucillus carcinoma or colloid  Paget’s disease  Inflammatory breast cancer  Metastatic breast cancer  Triple negative breast cancer
  • 6. EPIDEMIOLOGY  Breast cancer constitutes a major public health issue , resulting in over 4,00,000 annual deaths and about 4.4 million women living with this disease.  It accounts for 16% of all female cancers and 22.9% of invasive cancers in women.  18.2% of all cancer deaths in world wide, including both males and females, are from breast cancer.  There is an international/geographical variation in the incidence of breast cancer.  Incidence rates are higher in the developed countries than in the developing countries and japan.
  • 7. SYMPTOMS  A lump in a breast  A pain in the armpits or breast that does not seem to be related to the woman's menstrual period  Redness of the skin of the breast  A rash around (or on) one of the nipples  A swelling (lump) in one of the armpits  An area of thickened tissue in a breast  One of the nipples has a discharge; sometimes it may contain blood  The size or the shape of the breast changes  The nipple-skin or breast-skin may have started to peel, scale or flake.
  • 8. RISK FACTORS FOR BREAST CANCER Non-modifiable  Gender  Age(>45y)  Genetic changes of breast cancer  Family history of breast cancer  Female Personal history of breast cancer  Race and ethnicity  Dense breast tissue  Lobular carcinoma in situ(LCIS)  Menstrual periods  Diethyl still besterol exposure  Previous chest radiation Modifiable  Not having children  Contraceptives  Harmone therapy after menopause  Alcohol consumption  Breast feeding  Obesity  Physical exercise
  • 9. ETIOLOGY  General Aging Gender  Genetics Family history Inherited factors  Body Obesity Not having children High breast density Certain breast changes Menstrual history  Life style A sedentary life style Heavy drinking
  • 11. PATHOLOGY OF BREAST CANCER  Hereditary cancers are primarily caused by an inherited genetic defect.  Less than 0.3% of the population are carriers of a genetic mutation that has a large effect on cancer risk and these cause less than 3–10% of cancer.  Some of these syndromes include certain inherited mutations in the genes BRCA1 and BRCA2 with a more than 75% risk of breast cancer and ovarian cancer, and Hereditarynonpolyposiscolor ectal cancer (HNPCC or Lynch syndrome).
  • 12.  GENETICS  EPIGENETICS
  • 14. STAGES OF BREAST CANCER STAGES DESCRIPTION Stage-0 • Abnormal cells in the lining of the ducts(or) sections of the breast. • Results in increased risk of developing cancer in both breasts. Stage-1 • Invasive breast cancer , the cancerous cells are breaking through to or invading surrounding normal tissue. Stage-2a 2b • No tumour but there are cancerous cells in the lymph nodes , or there is a tumour that has grown. • Cancerous cells in the lymph nodes and/or tumour has grown. Stage-3 • Cancer has spread to lymph nodes near breastbone and chest wall. Stage-4 • Cancer has spread to other parts
  • 15. BREAST CANCER AND PREGNANCY Breast cancer and pregnancy can be classified into three main situations; these are (a) breast cancer that is detected during the evolution of pregnancy (b) breast cancer that is detected during lactation or postpartum, and (c) pregnancy in patients who have had a previous breast cancer. Cancer complicates approximately 1 per 1000 pregnancies and accounts for one-third of maternal deaths during gestation. The prevalence of breast cancer during pregnancy is increasing due to delayed onset of childbearing.
  • 16. DIAGNOSIS OF BREAST CANCER  PHYSICAL EXAM AND HISTORY:  MAMMOGRAM  ULTRASOUND EXAM  MRI (MAGNETIC RESONANCE IMAGING)  BLOOD CHEMISTRY STUDIES:  BIOPSY:  Excisional biopsy  Incisional biopsy  Core biopsy  Fine-needle aspiration (FNA) biopsy  Biopsy samples are tested for the following  ESTROGEN AND PROGESTERONE RECEPTOR TEST  HUMAN EPIDERMAL GROWTH FACTOR TYPE 2 RECEPTOR(HER2/neu)TEST  MULTIGENE TESTS
  • 18. SCREENING  Average –size lump found by women practicing occasional breast self exam.  Average –size lump found by women practicing regular breast self exam.  Average –size lump found by first mammogram.  Average –size lump found by getting regular mammograms.
  • 19. TREATMENT OF BREAST CANCER  Surgery Breast conserving or mastectomy , with lymph node examination(ALND or SLNB)  Chemotherapy Before or after surgery. Anthracyclins, Taxanes etc  Hormonal therapy SERMs, Als, LHRH analogues, oophrectomy  Targeted biological therapy Tratuzumab, new dual therapies very promising  Radiotherapy Teletherapy , brachytherapy, intraop RT (TARGIT trail)
  • 21. EARLY DETECTION  Early detection of breast cancer plays the leading role in reducing mortality rates and improving the patient’s prognosis(Elmore et al.,2005)  The survival rate is higher with early detection of breast cancer. However, with local invasion, the survival rate decreases and if it is diagnosed at the latest stage, only a very low numbers of patients will survive.  For primary prevention of breast cancer, women need to be adequately informed about risk factors and risk reduction strategies of breast cancer.
  • 22. CONCLUSION Management of breast cancer is a major challenge in resource limited countries. Efforts should be geared towards early diagnosis, prompt and standardized treatment to reduce the burden of advanced disease in women, majority of who are worse hit in the most productive part of their life time.